부산대학교 도서관

Vishnu VY; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India.; Lemmers RJLF; Department of Human Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Reyaz A; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India.; Mishra R; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India.; Ahmad T; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India.; van der Vliet PJ; Department of Human Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Kretkiewicz MM; Department of Human Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Macken WL; Department of Neuromuscular Diseases, Queen Square Institute of Neurology, University College London, London, UK.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Queen Square Centre for Neuromuscular Diseases, The National Hospital for Neurology and Neurosurgery, London, UK.; Efthymiou S; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; Dominik N; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; Morrow JM; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; Bhatia R; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India.; Wilson LA; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; Houlden H; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; Hanna MG; Department of Neuromuscular Diseases, Queen Square Institute of Neurology, University College London, London, UK. m.hanna@ucl.ac.uk.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Queen Square Centre for Neuromuscular Diseases, The National Hospital for Neurology and Neurosurgery, London, UK. m.hanna@ucl.ac.uk.; Bugiardini E; Department of Neuromuscular Diseases, Queen Square UCL Institute of Neurology and the National Hospital of Neurology and Neurosurgery, London, UK.; van der Maarel SM; Department of Human Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Srivastava MVP; Department of Neurology, All India Institute of Medical Sciences (AIIMS), Delhi, India. vasanthapadma123@gmail.com.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE