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Article

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

The Journal of dermatology - 1 Jan 2021

Sun Junhui, Chen Liang, Han Shuai, He Yang, Dumitru Alexandru George, Zhou Weibin, Cai Jiali, Qi Ming

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Share to Child, Preschool
Share to Ectodermal Dysplasia
Share to Ectodermal Dysplasia 1, Anhidrotic
Share to Ectodysplasins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33180991
DOI: 10.1111/1346-8138.15653

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

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Characterization of a novel gross deletion and insertion mutation in EDA gene causing hypohidrotic ectodermal dysplasia.PMID 33180991Read ↗

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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 ↗

Gene symbol: EDA. Disease: Ectodermal dysplasia.Semantic proximity Read ↗

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Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review.Semantic proximity Read ↗

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