Literature DB >> 15888179

Novel mutation of connexin 31 causing erythrokeratoderma variabilis.

L Feldmeyer, L Plantard, B Mevorah, M Huber, D Hohl.   

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Year:  2005        PMID： 15888179     DOI： 10.1111/j.1365-2133.2005.06561.x

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


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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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