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Article

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

Journal of dermatological science - 1 Jan 2008

Wattanasirichaigoon Duangrurdee, Suwannarat Pim, Thongpradit Supranee

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Share to Albinism, Oculocutaneous
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18036783
DOI: 10.1016/j.jdermsci.2007.10.004

Genes

OCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Two novel splice mutations of P gene in a Thai-Chinese patient with oculocutaneous albinism type II (OCA2).PMID 18036783Read ↗

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

Two novel mutations detected in Japanese patients with oculocutaneous albinism.Semantic proximity Read ↗

[Analysis of P gene variations among fourteen patients with oculocutaneous albinism type II].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 ↗

[Mutations and polymorphisms of the P gene associated with oculocutaneous albinism type II].Semantic proximity Read ↗

P gene mutations associated with oculocutaneous albinism type II (OCA2).Semantic proximity Read ↗

Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutationsSemantic proximity Read ↗

Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients.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 ↗

P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.Semantic proximity Read ↗

Oculocutaneous albinism type 3 (OCA3): analysis of two novel mutations in TYRP1 gene in two Chinese patients.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.Semantic proximity Read ↗

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