Literature DB >> 26046476

Case of X-linked hypohidrotic ectodermal dysplasia with a novel EDA missense mutation.

Masahito Yasuda1, Chikako Kishi1, Yoko Yokoyama1, Hiroo Amano1, Osamu Ishikawa1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2015        PMID： 26046476     DOI： 10.1111/1346-8138.12959

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


× No keyword cloud information.
  3 in total

1.  Gene screening facilitates diagnosis of complicated symptoms: A case report.

Authors:  Hong Duan; Di Zhang; Jing Cheng; Yu Lu; Huijun Yuan
Journal:  Mol Med Rep       Date:  2017-09-22       Impact factor: 2.952

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

Authors:  Xu Wang; Zhiyu Zhang; Shuo Yuan; Jiabao Ren; Hong Qu; Guozhong Zhang; Wenjing Chen; Shushen Zheng; Lingqiang Meng; Jiuping Bai; Qingqing Du; Dongru Yang; Wenjing Shen
Journal:  Medicine (Baltimore)       Date:  2020-03       Impact factor: 1.817

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

Authors:  Yang Han; Xiuli Wang; Liyun Zheng; Tingting Zhu; Yuwei Li; Jiaqi Hong; Congcong Xu; Peiguang Wang; Min Gao
Journal:  Front Genet       Date:  2020-02-04       Impact factor: 4.599
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.