Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles

Author:

Zernant Jana1,Ku¨lm Maigi2,Dharmaraj Sharola3,den Hollander Anneke I.4,Perrault Isabelle5,Preising Markus N.6,Lorenz Birgit6,Kaplan Josseline5,Cremers Frans P. M.4,Maumenee Irene7,Koenekoop Robert K.8,Allikmets Rando9

Affiliation:

1. From the Departments of Ophthalmology and

2. Asper Biotech, Ltd., Tartu, Estonia;

3. Department of Pediatric Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts; the

4. Department of Human Genetics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands;

5. Ho^pital Des Enfants Malades, Paris, France; the

6. Department of Pediatric Ophthalmology, Strabismology and Ophthalmogenetics, Klinikum, University of Regensburg, Regensburg, Germany; the

7. Johns Hopkins University, Baltimore, Maryland; and the

8. Montreal Children’s Hospital, McGill University Health Center, Montreal, Quebec, Canada.

9. From the Departments of Ophthalmology and10Pathology, Columbia University, New York, New York;

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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