부산대학교 도서관

Rots D; Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Genetics Laboratory, Children's Clinical University Hospital, Riga, Latvia.; Bouman A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; Yamada A; Cellular Memory Laboratory, RIKEN Cluster for Pioneering Research, RIKEN, Wako, Saitama, Japan.; Levy M; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada.; Dingemans AJM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; de Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Ruiterkamp-Versteeg M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; de Leeuw N; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Ockeloen CW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; de Boer E; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Kummeling J; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; van Bon B; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; van Bokhoven H; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Kasri NN; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Venselaar H; Department of Medical BioSciences, Radboudumc, Nijmegen, the Netherlands.; Alders M; Department of Human Genetics, Amsterdam UMC location University of Amsterdam, Amsterdam, the Netherlands; Amsterdam Reproduction and Development research institute, Amsterdam, the Netherlands.; Kerkhof J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada.; McConkey H; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada.; Kuechler A; Institute of Human Genetics, University Hospital Essen, Essen, Germany.; Elffers B; Cordaan, Amsterdam, the Netherlands; Department of Medical Care for Patients with Intellectual Disability, AMSTA, Amsterdam, the Netherlands.; van Beeck Calkoen R; Cordaan, Amsterdam, the Netherlands.; Hofman S; Evean Oostergouw, Zaandam, the Netherlands.; Smith A; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Valenzuela MI; Department of Clinical and Molecular Genetics and Rare Disease Unit Hospital Vall d'Hebron, Barcelona, Spain; Medicine Genetics Group, Vall Hebron Research Institute, Barcelona, Spain.; Srivastava S; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; Frazier Z; Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Maystadt I; Institut de Pathologie et de Génétique Centre de Génétique Humaineavenue G. Lemaître, 256041 Gosselies, Belgium.; Piscopo C; Medical and Laboratory Unit, Antonio cardarelli Hospital, via A.Cardarelli 9, 80131 Naples, Italy.; Merla G; Department of Molecular Medicine and Medical Biotechnology, University of Naples, Naples, Italy; Laboratory of Regulatory and Functional Genomics, fondazione IRCCS casa sollievo della sofferenza, san giovanni rotondo, Foggia, Italy.; Balasubramanian M; Division of Clinical Medicine, University of Sheffield, Sheffield, UK; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.; Santen GWE; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Metcalfe K; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Park SM; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Pasquier L; Reference Center for Rare Diseases, Hôpital Sud - CHU Rennes, Rennes, France.; Banka S; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Donnai D; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Weisberg D; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Strobl-Wildemann G; MVZ Humangenetik Ulm, Ulm, Germany.; Wagemans A; Maasveld, Koraal, Maastricht, the Netherlands; Department of Family Medicine, Faculty of Health, Medicine and Life Science, Maastricht University, Maastricht, the Netherlands.; Vreeburg M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Baralle D; Human Development and Health, Faculty of Medicine, University Hospital Southampton, Southampton, Hampshire, UK.; Foulds N; Wessex Regional Genetics Services, UHS NHS Foundation Trust, Southampton, United Kingdom.; Scurr I; Department of Clinical Genetics, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.; Brunetti-Pierri N; Department of Translational Medicine, Federico II University of Naples, Naples, Italy; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy; Scuola Superiore Meridionale (SSM, School of Advanced Studies), Genomics and Experimental Medicine Program, University of Naples Federico II, Naples, Italy.; van Hagen JM; Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Human Genetics, Amsterdam, the Netherlands.; Bijlsma EK; Department of Clinical Genetica, Leiden University Medical Center, Leiden, the Netherlands.; Hakonen AH; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Courage C; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Genevieve D; Université Montpellier, Unité INSERM U1183, Montpellier, France; Centre de reference Anomalies du développement, ERN ITHACA, Service de génétique Clinique, CHU Montpellier, Montpellier, France.; Pinson L; Centre de reference Anomalies du développement, ERN ITHACA, Service de génétique Clinique, CHU Montpellier, Montpellier, France.; Forzano F; Clinical Genetics Department 7th Floor Borough WingGuy's Hospital, Guy's & St Thomas' NHS Foundation TrustGreat Maze Pond, London, UK.; Deshpande C; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Kluskens ML; Prinsenstichting, Purmerend, the Netherlands.; Welling L; Prinsenstichting, Purmerend, the Netherlands.; Plomp AS; Department of Human Genetics, Amsterdam UMC location University of Amsterdam, Amsterdam, the Netherlands; Amsterdam Reproduction and Development research institute, Amsterdam, the Netherlands.; Vanhoutte EK; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Kalsner L; Department of Pediatrics, Division of Neurology, Connecticut Children's, University of Connecticut, Farmington, CT, USA.; Hol JA; Clinical Genetics Department, Erasmus Medical Centre, Rotterdam, the Netherlands.; Putoux A; Hospices Civils de Lyon, Service de Génétique - Centre de Référence Anomalies du Développement, Bron, France; Centre de Recherche en Neurosciences de Lyon, Équipe GENDEV, INSERM U1028 CNRS UMR5292, Université Claude Bernard Lyon 1, Lyon, France.; Lazier J; Regional Genetics Program, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Vasudevan P; Department of Clinical Genetics, University Hospitals of Leicester NHS Trust, Leicester, UK.; Ames E; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.; O'Shea J; Division of Pediatric Genetics, Metabolism, and Genomic Medicine, C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Fleischer J; Southern Illinois University School of Medicine, Department of Pediatrics, Springfield, IL, USA.; O'Connor M; Southern Illinois University School of Medicine, Department of Pediatrics, Springfield, IL, USA.; Pauly M; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.; Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.; Kiraly-Borri C; Genetic Health Western Australia, Department of Health King Edward Memorial Hospital, Subiaco, WA 6008, Australia.; Bouman A; Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands.; Barnett C; Paediatric and Reproductive Genetics Unit 8th Floor, Clarence Rieger Building Women's and Children's Hospital, 72 King William Road North, Adelaide, SA 5006, Australia.; Nezarati M; Genetics, North York General Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.; Borch L; Department of Medical Genetics, North York General Hospital, University of Toronto, Toronto, ON, Canada.; Beunders G; Department of Genetics, University Medical Center Groningen, Groningen, the Netherlands.; Özcan K; Neurodevelopmental Treatment Association Çocuk Fizyoterapistleri Derneği Bobath Terapistleri Derneği, Ankara, Turkey.; Miot S; Geriatrics department, Montpellier University Hospital, MUSE University, Montpellier, France; INSERM U1298, INM, Montpellier, France.; Volker-Touw CML; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; van Gassen KLI; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Cappuccio G; Department of Translational Medicine, Section of Pediatrics, Federico II University, Via Pansini 5, Naples, Italy; TIGEM (Telethon Institute of Genetics and Medicine), Via Campi Flegrei 34, 80078 Pozzuoli (NA), Italy.; Janssens K; Department of Medical Genetics, Antwerp University Hospital/University of Antwerp, Edegem, Wilrijk, Belgium.; Mor N; Sheba Cancer Research Center, Chaim Sheba Medical Center, Ramat Gan, Israel.; Shomer I; Sheba Cancer Research Center, Chaim Sheba Medical Center, Ramat Gan, Israel.; Dominissini D; Sheba Cancer Research Center, Chaim Sheba Medical Center, Ramat Gan, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Ramat Aviv, Israel.; Tedder ML; Greenwood Genetic Center, Greenwood, SC, USA.; Muir AM; GeneDx Inc., Gaithersburg, MD 20877, USA.; Sadikovic B; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada.; Brunner HG; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Vissers LELM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Shinkai Y; Cellular Memory Laboratory, RIKEN Cluster for Pioneering Research, RIKEN, Wako, Saitama, Japan. Electronic address: yshinkai@riken.jp.; Kleefstra T; Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, the Netherlands. Electronic address: t.kleefstra@erasmusmc.nl.

Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Lehtonen J; Centre for Molecular Medicine Norway (NCMM), University of Oslo, Oslo, Norway.; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Sulonen AM; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.; Almusa H; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.; Lehtokari VL; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Johari M; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.; Palva A; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.; Hakonen AH; Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.; Wartiovaara K; Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.; Lehesjoki AE; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Udd B; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Wallgren-Pettersson C; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Pelin K; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Molecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.; Savarese M; Folkhälsan Research Center, Folkhälsan Institute of Genetics, Helsinki, Finland.; Medicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Saarela J; Centre for Molecular Medicine Norway (NCMM), University of Oslo, Oslo, Norway. j.s.saarela@ncmm.uio.no.; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland. j.s.saarela@ncmm.uio.no.; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway. j.s.saarela@ncmm.uio.no.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

Pardo LM; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.; Aanicai R; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.; Zonic E; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.; Hakonen AH; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Zielske S; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.; Bauer P; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.; Department of Internal Medicine III - Hematology, Oncology, and Palliative Medicine, University of Rostock, Rostock, Germany.; Bertoli-Avella AM; Medical Genetics, Reporting & Research, CENTOGENE GmbH, Rostock, Germany.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Isohanni P; Hakonen AH; Euro L; Paetau I; Linnankivi T; Liukkonen E; Wallden T; Luostarinen L; Valanne L; Paetau A; Uusimaa J; Lönnqvist T; Suomalainen A; Pihko H

Neurology; 3/1/2011, Vol. 76 Issue 9, p811-815, 5p

Kuuluvainen L; Department of Medical and Clinical Genetics (L.K., S.M., M.P.), University of Helsinki and Helsinki University Hospital, Finland.; Mönkäre S; Department of Medical and Clinical Genetics (L.K., S.M., M.P.), University of Helsinki and Helsinki University Hospital, Finland.; Department of Medical Genetics, Turku University Hospital, Finland (S.M.).; Kokkonen H; Northern Finland Laboratory Centre NordLab and Medical Research Centre, Oulu University Hospital and University of Oulu, Finland (H.K.).; Zhao F; Department of Pathology, University of Helsinki, Finland (F.Z.).; Verkkoniemi-Ahola A; Department of Clinical Neurosciences (A.V.-A.), Helsinki University Hospital and University of Helsinki, Finland.; Schleutker J; Institute of Biomedicine, University of Turku and Department of Medical Genetics, Turku University Hospital, Finland (J.S.).; Hakonen AH; Department of Clinical Genetics (A.H.H.), Helsinki University Hospital and University of Helsinki, Finland.; Hartikainen P; Neurocenter, Neurology, Kuopio University Hospital, Finland (P.H.).; Pöyhönen M; Department of Medical and Clinical Genetics (L.K., S.M., M.P.), University of Helsinki and Helsinki University Hospital, Finland.; Myllykangas L; Department of Pathology (L.M.), University of Helsinki and Helsinki University Hospital, Finland.

Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0235266 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1524-4628 (Electronic) Linking ISSN: 00392499 NLM ISO Abbreviation: Stroke Subsets: MEDLINE

Hakonen AH; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Lehtonen J; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Folkhälsan Research Center, Helsinki, Finland.; Kivirikko S; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Keski-Filppula R; Department of Clinical Genetics, Oulu University Hospital, Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu, Oulu, Finland.; Moilanen J; Department of Clinical Genetics, Oulu University Hospital, Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu, Oulu, Finland.; Kivisaari R; HUS Medical Imaging Center, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Almusa H; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Jakkula E; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Saarela J; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Centre for Molecular Medicine Norway (NCMM), University of Oslo, Oslo, Norway.; HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Avela K; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Aittomäki K; Department of Clinical Genetics, HUSLAB, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Hakonen AH; Isohanni P; Paetau A; Herva R; Suomalainen A; Lönnqvist T; Hakonen, Anna H; Isohanni, Pirjo; Paetau, Anders; Herva, Riitta; Suomalainen, Anu; Lönnqvist, Tuula

Brain: A Journal of Neurology (BRAIN), Nov2007; 130(11): 3032-3040. (9p)

Hakonen AH; Department of Clinical Genetics, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Polvi A; Department of Clinical Genetics, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Saloranta C; Department of Clinical Genetics, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Paetau A; Department of Pathology, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Heikkilä P; Department of Pathology, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Almusa H; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Ellonen P; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Jakkula E; Department of Clinical Genetics, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Saarela J; Institute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland.; Aittomäki K; Department of Clinical Genetics, HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Esterhuizen K; Mitochondria Research Laboratory, Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.; Lindeque JZ; Mitochondria Research Laboratory, Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.; Mason S; Mitochondria Research Laboratory, Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.; van der Westhuizen FH; Mitochondria Research Laboratory, Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.; Suomalainen A; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Hakonen AH; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Carroll CJ; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Rodenburg RJ; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.; de Laat PB; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.; Janssen MCH; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.; Smeitink JAM; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.; Louw R; Mitochondria Research Laboratory, Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa. Electronic address: Roan.Louw@nwu.ac.za.

Publisher: Elsevier Science Country of Publication: Netherlands NLM ID: 100968751 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-8278 (Electronic) Linking ISSN: 15677249 NLM ISO Abbreviation: Mitochondrion Subsets: MEDLINE

Buzkova J; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Nikkanen J; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Ahola S; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Hakonen AH; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Sevastianova K; Department of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Minerva Foundation Institute for Medical Research, Helsinki, Finland.; Hovinen T; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Yki-Järvinen H; Department of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Minerva Foundation Institute for Medical Research, Helsinki, Finland.; Pietiläinen KH; Research Programs Unit, Diabetes and Obesity, Obesity Research Unit, University of Helsinki, Helsinki, Finland.; Abdominal Centre, Endocrinology, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland.; Lönnqvist T; Department of Child Neurology, Children's Hospital, University of Helsinki, Helsinki, Finland.; Velagapudi V; Metabolomics Unit, Institute for Molecular Medicine Finland FIMM, HiLIFE, University of Helsinki, Helsinki, Finland.; Carroll CJ; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.; Genetics Research Centre, Molecular and Clinical Sciences Institute, St. George's University of London, London, UK.; Suomalainen A; Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland anu.wartiovaara@helsinki.fi.; Department of Neurosciences, Helsinki University Hospital, Helsinki, Finland.; Neuroscience Centre, Helsinki Institute Life Science, University of Helsinki, Helsinki, Finland.

Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101487380 Publication Model: Print Cited Medium: Internet ISSN: 1757-4684 (Electronic) Linking ISSN: 17574676 NLM ISO Abbreviation: EMBO Mol Med Subsets: MEDLINE