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Article

X-Linked Recessive Atrophic Macular Degeneration from RPGR Mutation

1 Aug 2002

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Share to Neuroinflammation and Neurodegeneration Mechanisms
Share to Retinal Development and Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12160730
DOI: 10.1006/geno.2002.6815

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

X-Linked Recessive Atrophic Macular Degeneration from RPGR MutationPMID 12160730Read ↗

RPGR: part one of the X-linked retinitis pigmentosa story.Semantic proximity Read ↗

From onset to blindness: a comprehensive analysis of RPGR-associated X-linked retinopathy in a large cohort in China.Semantic proximity Read ↗

Severe Phenotypic Presentation of RPGR-associated X-linked Retinitis Pigmentosa in Female Carriers: Two Case Reports.Semantic proximity Read ↗

Novel variants of RPGR in X-linked retinitis pigmentosa families and genotype-phenotype correlation.Semantic proximity Read ↗

Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.Semantic proximity Read ↗

X-linked cone dystrophy with an uncommon tapetal-like sheen caused by a novel RPGR variant.Semantic proximity Read ↗

Phenotypic progression in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene.Semantic proximity Read ↗

A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa.Semantic proximity Read ↗

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female CarriersSemantic proximity Read ↗

Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.Semantic proximity Read ↗

RPGR and RP2: targets for the treatment of X-linked retinitis pigmentosa?Semantic proximity Read ↗

Exploring the Variable Phenotypes of RPGR Carrier Females in Assessing Their Potential for Retinal Gene TherapySemantic proximity Read ↗

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