Literature DB >> 18076698

Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.

J Zhao1, R Hua, X Zhao, Y Meng, Y Ao, Q Liu, D Shang, M Sun, W H-Y Lo, X Zhang.   

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Year:  2007        PMID： 18076698     DOI： 10.1111/j.1365-2133.2007.08383.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  2 in total

1.  A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia.

Authors:  Daxu Li; Ran Xu; Fumeng Huang; Biyuan Wang; Yu Tao; Zijian Jiang; Hairui Li; Jianfeng Yao; Peng Xu; Xiaokang Wu; Le Ren; Rui Zhang; John R Kelsoe; Jie Ma
Journal:  J Genet       Date:  2015-03       Impact factor: 1.166

2.  [Detection of EDA gene mutation and phenotypic analysis in patients with hypohidrotic ectodermal dysplasia].

Authors:  J Y Wu; M Yu; S C Sun; Z Z Fan; J L Zheng; L T Zhang; H L Feng; Y Liu; D Han
Journal:  Beijing Da Xue Xue Bao Yi Xue Ban       Date:  2020-12-09
  2 in total

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