Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosa.

Human molecular genetics - 1 Aug 1994

Souied E, Gerber S, Rozet J M, Bonneau D, Dufier J L, Ghazi I, Philip N, Soubrane G, Coscas G, Munnich A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Codon
Share to Genes, Dominant
Share to Genotype
Share to Point Mutation

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

Share to Polymorphism, Single-Stranded Conformational

Share to Retinitis Pigmentosa

Share to Rhodopsin

Source

Identifiers

PMID: 7987331
DOI: 10.1093/hmg/3.8.1433

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosa.PMID 7987331Read ↗

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

Rhodopsin mutations in inherited retinal dystrophies and dysfunctionsSemantic proximity Read ↗

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

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

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.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 ↗

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

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

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain.Semantic proximity Read ↗

Identification of a rhodopsin gene mutation in a large family with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.