Literature DB >> 20497287

A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis.

Z-X Wang, W-S Lu, H Li, D Lin, F-S Zhou, L-D Sun, S Yang, X-J Zhang.   

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Year:  2011        PMID： 20497287     DOI： 10.1111/j.1468-3083.2010.03691.x

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


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  2 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

2.  Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressiva.

Authors:  Changxing Li; Jingyao Liang; Pingjiao Chen; Kang Zeng; Rujun Xue; Xin Tian; Liuping Liang; Qi Wang; Minglan Shi; Xibao Zhang
Journal:  Mol Genet Genomic Med       Date:  2019-03-29       Impact factor: 2.183
  2 in total

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