Literature DB >> 29444360

Two EDA gene mutations in chinese patients with hypohidrotic ectodermal dysplasia.

X Feng1, C Weng1, T Wei1, J Sun1, F Huang2, P Yu1, M Qi1,3,4,5,6.   

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Year:  2018        PMID： 29444360     DOI： 10.1111/jdv.14874

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  4 in total

Review 1.  Ectodysplasin A/Ectodysplasin A Receptor System and Their Roles in Multiple Diseases.

Authors:  Zhensheng Cai; Xia Deng; Jue Jia; Dong Wang; Guoyue Yuan
Journal:  Front Physiol       Date:  2021-12-06       Impact factor: 4.566

2.  A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.

Authors:  Hongyu Zhang; Xuanting Kong; Jiabao Ren; Shuo Yuan; Chunyan Liu; Yan Hou; Ye Liu; Lingqiang Meng; Guozhong Zhang; Qingqing Du; Wenjing Shen
Journal:  Mol Genet Genomic Med       Date:  2021-05-04       Impact factor: 2.183

3.  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

4.  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
  4 in total

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