IQCB1Mutations in Patients with Leber Congenital Amaurosis

Author:

Estrada-Cuzcano Alejandro1,Koenekoop Robert K.2,Coppieters Frauke3,Kohl Susanne4,Lopez Irma2,Collin Rob W. J.1,De Baere Elfride B. W.3,Roeleveld Debbie5,Marek Jonah2,Bernd Antje4,Rohrschneider Klaus6,van den Born L. Ingeborgh7,Meire Françoise8,Maumenee Irene H.9,Jacobson Samuel G.10,Hoyng Carel B.11,Zrenner Eberhart4,Cremers Frans P. M.12,den Hollander Anneke I.1

Affiliation:

1. From the Departments of Human Genetics and 2Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands; 3Nijmegen Center of Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands;

2. McGill Ocular Genetics Centre, McGill University Health Centre, Montreal, Canada;

3. Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium;

4. Department of Ophthalmology, University of Tübingen, Tübingen, Germany;

5. From the Departments of Human Genetics and

6. Department of Ophthalmology, University of Heidelberg, Heidelberg, Germany;

7. Rotterdam Eye Hospital, Rotterdam, The Netherlands;

8. HUDERF-Erasme Hospital Brussels, University Hospital of the Free University of Brussels, Brussels, Belgium;

9. Department of Ophthalmology, University of Illinois Eye and Ear Infirmary, Chicago, Illinois; and

10. Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania.

11. Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands;

12. From the Departments of Human Genetics and 3Nijmegen Center of Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands;

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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