Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation ofRBP3Is Associated With High Myopia and Retinal Dystrophy-Reference-Cited by-同舟云学术

Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation ofRBP3Is Associated With High Myopia and Retinal Dystrophy

Published:2015-04-10 Issue:4 Volume:56 Page:2358
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Arno Gavin¹,Hull Sarah¹,Robson Anthony G.¹,Holder Graham E.¹,Cheetham Michael E.²,Webster Andrew R.¹,Plagnol Vincent³,Moore Anthony T.⁴

Affiliation:

1. UCL Institute of Ophthalmology, London, United Kingdom 2Moorfields Eye Hospital, London, United Kingdom

2. UCL Institute of Ophthalmology, London, United Kingdom

3. University College London Genetics Institute, London, United Kingdom

4. UCL Institute of Ophthalmology, London, United Kingdom 2Moorfields Eye Hospital, London, United Kingdom 4Ophthalmology Department, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom 5Department of Ophthalmology, University of Cali

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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