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Article

Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.

Experimental dermatology - 1 Aug 2003

Hashiguchi Takaki, Yotsumoto Shinichi, Kanzaki Tamotsu

Abstract excerpt

X-linked hypohidrotic ectodermal dysplasia (XLHED; OMIM 305100) is characterized by sparse hair, abnormal teeth and decreased sweating as a result of abnormal development of the sweat glands. Mutations in the ED1 gene, which encodes ectodysplasin-A (EDA), are responsible for XLHED. Ectodysplasin-...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12930312
DOI: 10.1034/j.1600-0625.2002.120423.x

Genes

EDA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12930312-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.PMID 12930312Read ↗

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