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Article

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.

Nature genetics - 1 Dec 1999

Morimura H, Saindelle-Ribeaudeau F, Berson E L, Dryja T P

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10581022
DOI: 10.1038/70496

Genes

RGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.PMID 10581022Read ↗

RGR variants in different forms of retinal diseases: The undetermined role of truncation mutations.Semantic proximity Read ↗

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Identical mutation in a novel retinal gene causes progressive rod–cone degeneration in dogs and retinitis pigmentosa in humansSemantic proximity Read ↗

Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations.Semantic proximity Read ↗

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1.Semantic proximity Read ↗

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaSemantic proximity Read ↗

Rhodopsin mutation G109R in a family with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.Semantic proximity Read ↗

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections.Semantic proximity Read ↗

Rhodopsin mutations in a Scottish retinitis pigmentosa population, including a novel splice site mutation in intron four.Semantic proximity Read ↗

Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosaSemantic proximity Read ↗

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