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

[A Chinese family with autosomal dominant retinitis pigmentosa and a pro347Leu rhodopsin gene mutation].

Chinese medical journal - 1 Jun 2000

Yang H, Luo C, Zhou J, Yan M

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 Mutation
Share to Pedigree
Share to Retinitis Pigmentosa

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

Share to Rhodopsin

Source

Identifiers

PMID: 11775885

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

[A Chinese family with autosomal dominant retinitis pigmentosa and a pro347Leu rhodopsin gene mutation].PMID 11775885Read ↗

[A novel rhodopsin E341ter mutation in patients with retinitis pigmentosa and corresponding clinical phenotype].Semantic proximity Read ↗

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

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

[Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa].Semantic proximity Read ↗

Rhodopsin mutations in Chinese patients with retinitis pigmentosa.Semantic proximity Read ↗

[Molecular genetic analysis for Japanese patients with autosomal dominant retinitis pigmentosa].Semantic proximity Read ↗

Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

[Recent progress in molecular genetics and gene therapy for retinitis pigmentosa].Semantic proximity Read ↗

[Analysis of C2ORF71 gene variant in a Chinese patient with retinitis pigmentosa].Semantic proximity Read ↗

[Genotype-phenotype correlation in Chinese patients with retinitis pigmentosa due to rhodopsin mutation].Semantic proximity Read ↗

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

Autosomal dominant retinitis pigmentosa in a five-generation pedigree in People's Republic of China.Semantic proximity Read ↗

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