Literature DB >> 17573869

Erythrokeratoderma variabilis without GJB3 or GJB4 mutation: a review of Japanese patients.

M Nakamura.   

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Year:  2007        PMID： 17573869     DOI： 10.1111/j.1365-2133.2007.08023.x

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


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  2 in total

Review 1.  Connexin channels in congenital skin disorders.

Authors:  Evelyn Lilly; Caterina Sellitto; Leonard M Milstone; Thomas W White
Journal:  Semin Cell Dev Biol       Date:  2016-01-13       Impact factor: 7.727

2.  Erythrokeratodermia variabilis: Two case reports.

Authors:  Ayse Serap Karadag; Serap Gunes Bilgili; Omer Calka; Irfan Bayram
Journal:  Indian Dermatol Online J       Date:  2013-10
  2 in total

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