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Article

Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin.

Human molecular genetics - 1 Jun 1993

Kranich H, Bartkowski S, Denton M J, Krey S, Dickinson P, Duvigneau C, Gal A

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 8353500
DOI: 10.1093/hmg/2.6.813

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin.PMID 8353500Read ↗

A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease.Semantic proximity Read ↗

Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutation.Semantic proximity Read ↗

Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.Semantic proximity Read ↗

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A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family.Semantic proximity Read ↗

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Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.Semantic proximity Read ↗

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Rhodopsin splice site sequence changes in retinitis pigmentosa and their effect at the mRNA level.Semantic proximity Read ↗

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin.Semantic proximity Read ↗

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

Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

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