Literature DB >> 27443954

A novel large deletion that encompasses EDA and the downstream gene AWAT2 causes X-linked hypohidrotic/anhidrotic ectodermal dysplasia.

Ajay K Chaudhary1, V H Sankar2, Murali D Bashyam3.   

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Year:  2016        PMID： 27443954     DOI： 10.1016/j.jdermsci.2016.06.012

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN： 0923-1811            Impact factor:   4.563


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  3 in total

1.  Genetic diagnosis for X-linked hypohidrotic ectodermal dysplasia family with a novel Ectodysplasin A gene mutation.

Authors:  Xin Ma; Xue Lv; Hong-Yan Liu; Xing Wu; Li Wang; Hao Li; Hai-Yan Chou
Journal:  J Clin Lab Anal       Date:  2018-07-13       Impact factor: 2.352

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

Authors:  Binghui Zeng; Xue Xiao; Sijie Li; Hui Lu; Jiaxuan Lu; Ling Zhu; Dongsheng Yu; Wei Zhao
Journal:  Genes (Basel)       Date:  2016-09-19       Impact factor: 4.096

3.  X-Linked Hypohidrotic Ectodermal Dysplasia in Crossbred Beef Cattle Due to a Large Deletion in EDA.

Authors:  Donal O'Toole; Irene M Häfliger; Fabienne Leuthard; Brant Schumaker; Lynn Steadman; Brian Murphy; Cord Drögemüller; Tosso Leeb
Journal:  Animals (Basel)       Date:  2021-03-02       Impact factor: 2.752
  3 in total

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