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Article

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

The British journal of dermatology - 1 Mar 2008

Zhao J, Hua R, Zhao X, Meng Y, Ao Y, Liu Q, Shang D, Sun M, Lo W H-Y, Zhang X

Abstract excerpt

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Topics

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Share to Amino Acid Sequence
Share to Chromosomes, Human, X
Share to Ectodermal Dysplasia
Share to Ectodysplasins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Mutation

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Source

Identifiers

PMID: 18076698
DOI: 10.1111/j.1365-2133.2007.08383.x

Genes

EDA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.PMID 18076698Read ↗

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 ↗

Mutation Screening of the EDA Gene in Seven Chinese 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 ↗

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

Characterization of a novel gross deletion and insertion mutation in EDA gene causing hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

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

EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature.Semantic proximity Read ↗

Novel EDA mutations cause X-linked hypohidrotic ectodermal dysplasia: the first study from Venezuela.Semantic proximity Read ↗

Identification of a novel mutation of the EDA gene in X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

[Analysis of EDA gene mutation for a family affected with X-linked hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

Identification of six novel mutations in EDA from 20 hypohidrotic ectodermal dysplasia families.Semantic proximity Read ↗

Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands.Semantic proximity Read ↗

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