Literature DB >> 21950330

Mutation analysis of GJB3 and GJB4 in Chinese patients with erythrokeratodermia variabilis.

Hong Liu, Hong Liu, Xi-An Fu, Yong-Xiang Yu, Gui-Zhi Zhou, Xian-Mei Lu, Hong-Qing Tian, Chang-Ping Yu, Zhong-Xiang Shi, Mei-Ling Yu, Fu-Ren Zhang.   

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Year:  2011        PMID： 21950330     DOI： 10.1111/j.1346-8138.2011.01314.x

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


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  1 in total

1.  A Connexin Gene (GJB3) Mutation in a Chinese Family With Erythrokeratodermia Variabilis, Ichthyosis and Nonsyndromic Hearing Loss: Case Report and Mutations Update.

Authors:  Yajuan Gao; Qianli Zhang; Shiyu Zhang; Lu Yang; Yaping Liu; Yuehua Liu; Tao Wang
Journal:  Front Genet       Date:  2022-05-23       Impact factor: 4.772
  1 in total

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