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Article

A novel member of a zinc transporter family is defective in acrodermatitis enteropathica.

American journal of human genetics - 1 Jul 2002

Wang Kun, Zhou Bing, Kuo Yien-Ming, Zemansky Jason, Gitschier Jane

Abstract excerpt

The rare inherited condition acrodermatitis enteropathica (AE) results from a defect in the absorption of dietary zinc. Recently, we used homozygosity mapping in consanguineous Middle Eastern kindreds to localize the AE gene to an approximately 3.5-cM region on 8q24. In this article, we identify...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12032886
DOI: 10.1086/341125
PMCID: PMC419995

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12032886-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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