Leber Congenital Amaurosis Caused by an RPGRIP1 Mutation Shows Treatment Potential
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference24 articles.
1. Recent advances in early-onset severe retinal degeneration: more than just basic research;Preising;Trends Mol Med,2004
2. Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis;den Hollander;Am J Hum Genet,2006
3. Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness;Acland;Mol Ther,2005
4. Pharmacological and rAAV gene therapy rescue of visual functions in a blind mouse model of Leber congenital amaurosis;Batten;Plos Med,2005
5. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP;Pawlyk;Invest Ophthalmol Vis Sci,2005
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2. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022
3. Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype–Phenotype Correlation in 228 Patients;Frontiers in Cell and Developmental Biology;2021-10-14
4. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021-09-25
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