Gene Therapy in X-linked Retinitis Pigmentosa Due to Defects in RPGR
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference61 articles.
1. A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3);Meindl;Nat Genet,1996
2. RPGR isoforms in photoreceptor connecting cilia and the transitional zone of motile cilia;Hong;Invest Ophthalmol Vis Sci,2003
3. Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa;Vervoort;Nat Genet,2000
4. Complex expression pattern of RPGR reveals a role for purine-rich exonic splicing enhancers;Hong;Invest Ophthalmol Vis Sci,2002
5. Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation;Iannaccone;J Med Genet,2003
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