부산대학교 도서관

Alessandro Bitto; Takashi K Ito; Victor V Pineda; Nicolas J LeTexier; Heather Z Huang; Elissa Sutlief; Herman Tung; Nicholas Vizzini; Belle Chen; Kaleb Smith; Daniel Meza; Masanao Yajima; Richard P Beyer; Kathleen F Kerr; Daniel J Davis; Catherine H Gillespie; Jessica M Snyder; Piper M Treuting; Matt Kaeberlein

eLife, Vol 5 (2016)

Méjécase, C.; Mohand‐Saïd, S.; El Shamieh, S.; Antonio, A.; Condroyer, C.; Blanchard, S.; Letexier, M.; Saraiva, J.‐P.; Sahel, J.‐A.; Audo, I.; Zeitz, C.

Clinical Genetics. Mar 01, 2018 93(3):707-711

Neuillé, M.; Malaichamy, S.; Vadalà, M.; Michiels, C.; Condroyer, C.; Sachidanandam, R.; Srilekha, S.; Arokiasamy, T.; Letexier, M.; Démontant, V.; Sahel, J.-A.; Sen, P.; Audo, I.; Soumittra, N.; Zeitz, C.

Clinical Genetics. Jun 01, 2016 89(6):690-699

Bitto, Alessandro; Ito, Takashi K.; Pineda, Victor V.; LeTexier, Nicolas J.; Huang, Heather Z.; Sutlief, Elissa; Tung, Herman; Vizzini, Nicholas; Chen, Belle; Smith, Kaleb; Meza, Daniel; Yajima, Masanao; Beyer, Richard P.; Kerr, Kathleen F.; Davis, Daniel J.; Gillespie, Catherine H.; Snyder, Jessica M.; Treuting, Piper M.; Kaeberlein, Matt

eLife. August 23, 2016, Vol. 5

Letexier, D; Peroni, O; Pinteur, C; Beylot, M

In Diabetes and Metabolism 2005 31(6):558-566

Large, V; Peroni, O; Letexier, D; Ray, H; Beylot, M

In Diabetes and Metabolism 2004 30(4):294-309

Audo Isabelle; Bujakowska Kinga M; Léveillard Thierry; Mohand-Saïd Saddek; Lancelot Marie-Elise; Germain Aurore; Antonio Aline; Michiels Christelle; Saraiva Jean-Paul; Letexier Mélanie; Sahel José-Alain; Bhattacharya Shomi S; Zeitz Christina

Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 8 (2012)

Solaguren-Beascoa M; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.; Bujakowska KM; Department of Ophthalmology, Ocular Genomics Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, USA.; Méjécase C; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Emmenegger L; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Orhan E; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Neuillé M; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Mohand-Saïd S; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, INSERM-DGOS, CIC 1423, Paris, France.; Condroyer C; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Lancelot ME; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Michiels C; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Demontant V; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Antonio A; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Letexier M; IntegraGen SA, Evry, France.; Saraiva JP; IntegraGen SA, Evry, France.; Lonjou C; Plateforme Post-Génomique P3S, Hôpital Pitié Salpêtrière, Paris, France.; Carpentier W; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Plateforme Post-Génomique P3S, Hôpital Pitié Salpêtrière, Paris, France.; Léveillard T; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Pierce EA; Department of Ophthalmology, Ocular Genomics Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, USA.; Dollfus H; Centre de Référence Pour les Affections Rares en Génétique Ophtalmologique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Laboratoire UMRS_1112, Institut de Génétique Médicale d'Alsace, Université de Strasbourg, Strasbourg, France.; Sahel JA; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, INSERM-DGOS, CIC 1423, Paris, France.; Fondation Ophtalmologique Adolphe de Rothschild, Paris, France.; Department of Ophthalmology, The University of Pittsburgh School of Medicine University, Pittsburgh, USA.; Académie des Sciences-Institut de France, Paris, France.; Bhattacharya SS; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; UCL-Institute of Ophthalmology, London, UK.; Department of Cellular Therapy and Regenerative Medicine, Andalusian Centre for Molecular Biology and Regenerative Medicine (CABIMER), Seville, Spain.; Audo I; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.; Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, INSERM-DGOS, CIC 1423, Paris, France.; UCL-Institute of Ophthalmology, London, UK.; Zeitz C; Department of Genetics, Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

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