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Article

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin.

Genomics - 1 Dec 1991

Farrar G J, Kenna P, Redmond R, Shiels D, McWilliam P, Humphries M M, Sharp E M, Jordan S, Kumar-Singh R, Humphries P

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PMID: 1783387

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

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Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin.PMID 1783387Read ↗

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Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4.Semantic proximity Read ↗

Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.Semantic proximity Read ↗

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Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.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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