A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia

A mutation in the epithelial morphogen gene ectodysplasin-A1 (EDA1) is responsible for the disorder X-linked hypohidrotic ectodermal dysplasia (XLHED), the most common form of ectodermal dysplasia. XLHED is characterized by impaired development of hair, eccrine sweat glands, and teeth. This study ai...

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Detalles Bibliográficos
Autores principales: Wang, Xu, Zhang, Zhiyu, Yuan, Shuo, Ren, Jiabao, Qu, Hong, Zhang, Guozhong, Chen, Wenjing, Zheng, Shushen, Meng, Lingqiang, Bai, Jiuping, Du, Qingqing, Yang, Dongru, Shen, Wenjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220389/
https://www.ncbi.nlm.nih.gov/pubmed/32176048
http://dx.doi.org/10.1097/MD.0000000000019244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220389/
https://www.ncbi.nlm.nih.gov/pubmed/32176048
http://dx.doi.org/10.1097/MD.0000000000019244

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