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...

Descripción completa

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

Ejemplares similares

Ejemplares similares