EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature-Reference-Cited by-同舟云学术

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EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature

Published:2015 Issue:3 Volume:14 Page:10344-10351
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Huang S.X.,Liang J.L.,Sui W.G.,Lin H.,Xue W.,Chen J.J.,Zhang Y.,Gong W.W.,Dai Y.,Ou M.L.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2015/vol14-3/pdf/gmr6656.pdf

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia;BMC Oral Health;2024-01-27

2. Next generation sequencing panel target genes: possible diagnostic tool for ectodermal dysplasia related diseases;Italian Journal of Dermatology and Venereology;2023-03

3. Hypohidrotic ectodermal dysplasia: a case report;Annals of Medicine & Surgery;2023-02-17

4. Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia;Children;2022-09-06

5. Three Variants Affecting Exon 1 of Ectodysplasin A Cause X-Linked Hypohidrotic Ectodermal Dysplasia: Clinical and Molecular Characteristics;Frontiers in Genetics;2022-07-06

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