The molecular basis of human retinal and vitreoretinal diseases
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
Reference409 articles.
1. EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa;Abd El-Aziz;Nat. Genet.,2008
2. Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases;Abid;J. Med. 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. Gene therapy restores vision in a canine model of childhood blindness;Acland;Nat. Genet.,2001
5. A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness;al Jandal;Hum. Mutat.,1999
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