[41] In vivo assessment of photoreceptor function in human diseases caused by photoreceptor-specific gene mutations
Author:
Publisher
Elsevier
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1. Molecular genetics of retinitis pigmentosa
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1. A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration;Frontiers in Cell and Developmental Biology;2021-08-17
2. Bright-Flash Electroretinogram;Encyclopedia of Ophthalmology;2018
3. PRPH2 (RDS);Retinal Dystrophy Gene Atlas;2018
4. Bright-Flash Electroretinogram;Encyclopedia of Ophthalmology;2015
5. The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene;Progress in Retinal and Eye Research;2008-03
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