Rod and Cone Opsin Mislocalization in an Autopsy Eye From a Carrier of X-linked Retinitis Pigmentosa With a Gly436Asp Mutation in the RPGR Gene
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference5 articles.
1. A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model of X-linked retinitis pigmentosa (RP3);Hong;Proc Natl Acad Sci,2000
2. X-linked retinitis pigmentosa;Sharon;Invest Ophthalmol Vis Sci,2000
3. Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15;Aguirre;Exp Eye Res,2002
4. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa;Sharon;Am J Hum Genet,2003
5. Histopathologic-genotypic correlations in retinitis pigmentosa and allied diseases;Ben-Arie-Weintrob;Ophthalmol Genet,2005
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1. Gene Therapy Trial on X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR;Essentials in Ophthalmology;2024
2. Retinal degeneration in rpgra mutant zebrafish;Frontiers in Cell and Developmental Biology;2023-06-07
3. Emerging gene therapy products for RPGR-associated X-linked retinitis pigmentosa;Expert Opinion on Emerging Drugs;2022-10-02
4. Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy;The American Journal of Human Genetics;2020-06
5. Disrupted Plasma Membrane Protein Homeostasis in a Xenopus Laevis Model of Retinitis Pigmentosa;The Journal of Neuroscience;2019-05-06
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