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Article

Molecular basis of oculocutaneous albinism.

The Journal of investigative dermatology - 1 Nov 1994

Oetting W S, King R A

Abstract excerpt

Oculocutaneous albinism (OCA) is a complex group of genetic disorders that have historically been defined by clinical and biochemical methods. Recent advances in the molecular biology of pigmentation have greatly increased our understanding of the complexity of this group of disorders. To date, two different types of OCA (OCA1 and OCA2) have been mapped to specific chromosomal regions. Mutations have been found...

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Source

Identifiers

PMID: 7963676
DOI: 10.1111/1523-1747.ep12399447

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.

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