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

Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency.

Vision research - 1 Jan 2004

Ueyama Hisao, Kuwayama Shigeki, Imai Hiroo, Oda Sanae, Nishida Yasuhiro, Tanabe Shoko, Shichida Yoshinori, Yamade Shinichi

Abstract excerpt

The L-cone/M-cone visual pigment gene arrays were analyzed in 125 Japanese males with protan color-vision deficiency. Arrays were successfully determined in 62/65 subjects with protanopia and 57/60 protanomaly subjects. Among the 62 protanopia subjects, 48 (77%) had an array consisting of a single 5' L-M hybrid gene (PS-array) or a 5' L-M hybrid gene followed by an M gene(s) that was structurally identical to the...

Read the complete abstract on PubMed

Topics

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

Share to Color Vision Defects
Share to Exons

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

Share to Genotype

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single-Stranded Conformational

Share to Retinal Pigments

Share to Spectrum Analysis

Source

Identifiers

PMID: 15208011
DOI: 10.1016/j.visres.2004.04.011

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

Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency.PMID 15208011Read ↗

The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes.Semantic proximity Read ↗

A new subset of deutan colour vision defect associated with an L/M visual pigment gene array of normal order and -71C substitution in the Japanese population.Semantic proximity Read ↗

Selective cone dystrophy with protan genotype.Semantic proximity Read ↗

Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.Semantic proximity Read ↗

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.Semantic proximity Read ↗

[Inherited colour vision deficiencies--from Dalton to molecular genetics].Semantic proximity Read ↗

[A protanomalous female whose genotype of red/green visual pigment genes was determined by molecular analysis of her family members].Semantic proximity Read ↗

An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency.Semantic proximity Read ↗

Progressive cone dystrophy with deutan genotype and phenotype.Semantic proximity Read ↗

Macular dystrophy with protan genotype and phenotype studied with cone type specific ERGs.Semantic proximity Read ↗

Genetics of color vision deficiencies.Semantic proximity Read ↗

Color-deficient cone mosaics associated with Xq28 opsin mutations: a stop codon versus gene deletions.Semantic proximity Read ↗

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