CRB1Heterozygotes with Regional Retinal Dysfunction: Implications for Genetic Testing of Leber Congenital Amaurosis

Author:

Yzer Suzanne1,Fishman Gerald A.2,Racine Julie3,Al-Zuhaibi Sana4,Chakor Hadi3,Dorfman Allison3,Szlyk Janet2,Lachapelle Pierre3,van den Born L. Ingeborgh5,Allikmets Rando6,Lopez Irma4,Cremers Frans P. M.7,Koenekoop Robert K.4

Affiliation:

1. From the McGill Ocular Genetics Centre, Division of Ophthalmology, and the2Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands;3Rotterdam Eye Hospital, Rotterdam, The Netherlands; and the

2. Department of Ophthalmology, University of Illinois, Chicago, Illinois; the

3. McGill Visual Physiology Laboratory, Montreal Children’s Hospital Research Institute, McGill University Health Centre, Montreal, Quebec, Canada; the

4. From the McGill Ocular Genetics Centre, Division of Ophthalmology, and the

5. Rotterdam Eye Hospital, Rotterdam, The Netherlands; and the

6. Departments of Ophthalmology and Pathology, Columbia University, New York, New York.

7. Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands;

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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