RDH12andRPE65, Visual Cycle Genes Causing Leber Congenital Amaurosis, Differ in Disease Expression

Author:

Jacobson Samuel G.1,Cideciyan Artur V.1,Aleman Tomas S.1,Sumaroka Alexander1,Schwartz Sharon B.1,Windsor Elizabeth A. M.1,Roman Alejandro J.1,Heon Elise2,Stone Edwin M.3,Thompson Debra A.4

Affiliation:

1. From the Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania; the

2. Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Canada;

3. Howard Hughes Medical Institute and the4Department of Ophthalmology, University of Iowa Hospitals and Clinics, Iowa City, Iowa; the

4. Departments of Ophthalmology and Visual Sciences and6Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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1. RDH12 retinopathy: clinical features, biology, genetics and future directions;Ophthalmic Genetics;2022-05-02

2. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

3. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021-09-25

4. OCT Imaging in Infants;Seminars in Ophthalmology;2021-09-09

5. Leber’s Congenital Amaurosis: Current Concepts of Genotype-Phenotype Correlations;Genes;2021-08-19

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