Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations

Sarah Hull; Graham E Holder; Anthony G Robson; Rajarshi Mukherjee; Michel Michaelides; Andrew R Webster; Anthony T Moore

doi:10.1136/bjophthalmol-2015-308019

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Clinical science

Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations

Authors

Sarah Hull UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Graham E Holder UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Anthony G Robson UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Rajarshi Mukherjee UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Michel Michaelides UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Andrew R Webster UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Anthony T Moore UCL Institute of Ophthalmology, London, UK Moorfields Eye Hospital, London, UK Department of Ophthalmology, University of California, San Francisco Medical Centre, California, USA PubMed articles Google scholar articles

Correspondence to Professor Tony Moore, Ophthalmology Department, UCSF School of Medicine, Koret Vision Centre 10 Koret Way, San Francisco, CA 94143, USA; tony.moore{at}ucsf.edu

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Citation

Hull S, Holder GE, Robson AG, et al

Preserved visual function in retinal dystrophy due to hypomorphic RPE65 mutations

British Journal of Ophthalmology 2016;100:1499-1505.

Publication history

Received October 26, 2015
Revised January 12, 2016
Accepted January 25, 2016
First published February 23, 2016.

Online issue publication

November 28, 2016

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