A Novel Missense Mutation in Collagenous Domain of EDA Gene in a Chinese Family with X-linked Hypohidrotic Ectodermal Dysplasia

Overview

Journal J Genet

Specialty Genetics

Date 2015 Apr 8

PMID 25846883

Citations 4

Authors

Daxu Li

Ran Xu

Fumeng Huang

Biyuan Wang

Yu Tao

Zijian Jiang

Hairui Li

Jianfeng Yao

Peng Xu

Xiaokang Wu

Le Ren

Rui Zhang

John R Kelsoe

Jie Ma

Affiliations

Soon will be listed here.

Citing Articles

Mutations Causing X-Linked Recessive Oligodontia with Variable Expression.

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Pathogenic Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype-Phenotype: A Correlation Analysis.

Han Y, Wang X, Zheng L, Zhu T, Li Y, Hong J Front Genet. 2020; 11:21.

PMID: 32117440 PMC: 7010634. DOI: 10.3389/fgene.2020.00021.

EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.

Martinez-Romero M, Ballesta-Martinez M, Lopez-Gonzalez V, Sanchez-Soler M, Serrano-Anton A, Barreda-Sanchez M Orphanet J Rare Dis. 2019; 14(1):281.

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Phenotypic Features and Salivary Parameters in Patients with Ectodermal Dysplasia: Report of Three Cases.

Gomes M, Sichi L, Giannasi L, Amorim J, da Rocha J, Koga-Ito C Case Rep Dent. 2018; 2018:2409212.

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Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.

Zeng B, Xiao X, Li S, Lu H, Lu J, Zhu L Genes (Basel). 2016; 7(9).

PMID: 27657131 PMC: 5042395. DOI: 10.3390/genes7090065.

References

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