Extended functional rescue following AAV gene therapy in a canine model of LRIT3-congenital stationary night blindness
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
Reference35 articles.
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3. Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness;Audo;American Journal of Human Genetics,2012
4. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Bech-Hansen;Nature Genetics,2000
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1. Gene therapy and therapeutic editing with outer or inner retina animal models;Vision Research;2023-12
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