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Article

Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African-Americans.

Human mutation - 1 Jan 1996

Durham-Pierre D, King R A, Naber J M, Laken S, Brilliant M H

Abstract excerpt

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Share to Albinism, Oculocutaneous
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 8723691
DOI: 10.1002/(SICI)1098-1004(1996)7:4<370::AID-HUMU15>3.0.CO;2-#

Genes

OCA2

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→

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Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African-Americans.PMID 8723691Read ↗

Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.Semantic proximity Read ↗

Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene.Semantic proximity Read ↗

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2).Semantic proximity Read ↗

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism.Semantic proximity Read ↗

Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.Semantic proximity Read ↗

[A de novo mutation of P gene causes oculocutaneous albinism type 2 with prenatal diagnosis].Semantic proximity Read ↗

Unsuspected consequences of synonymous and missense variants in<i>OCA2</i>can be detected in blood cell RNA samples of patients with albinismSemantic proximity Read ↗

Two novel splice mutations of P gene in a Thai-Chinese patient with oculocutaneous albinism type II (OCA2).Semantic proximity Read ↗

Curation of OCA2 Variants of Uncertain Significance From Chinese Oculocutaneous Albinism Patients Based on Multiplex Assays.Semantic proximity Read ↗

Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.Semantic proximity Read ↗

Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2).Semantic proximity Read ↗

A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.Semantic proximity Read ↗

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