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Article

Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia.

Archives of dermatological research - 1 Apr 2003

Zhang Xue-Jun, Chen Jian-Jun, Song Ying-Xue, Yang Sen, Xiong Xiao-Yan, Zhang An-Ping, He Ping-Ping, Gao Min, Li Yue-Bin, Lin Da, Huang Wei

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Share to Asian People
Share to Chromosomes, Human, X
Share to Ectodermal Dysplasia
Share to Ectodysplasins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Membrane Proteins

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Share to Recombination, Genetic

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Identifiers

PMID: 12682853
DOI: 10.1007/s00403-003-0394-7

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

Related research

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Research trail→

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Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia.PMID 12682853Read ↗

Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia.Semantic proximity Read ↗

[Genetical diagnosis in a family with X-linked hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

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

A novel arginine-->Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia.Semantic proximity Read ↗

Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia.Semantic proximity Read ↗

A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family.Semantic proximity Read ↗

[Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Identified a novel splicing mutation at EDA gene in a hypohidrotic ectodermal dysplasia pedigree.Semantic proximity Read ↗

Mutation in the ED1 gene, Ala349Thr, in a Korean patient with X-linked hypohidrotic ectodermal dysplasia developing de novo.Semantic proximity Read ↗

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