An Unusual Missense Mutation in the GJB3 Gene Resulting in Severe Erythrokeratodermia Variabilis

By Glatz Martin   van Steensel Maurice A. M.   van Geel Michel   Steijlen Peter M.   Wolf Peter  

Acta Dermato-Venereologica, Vol. 91, Iss. 6, 2011-11 ,pp. : 714-715

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Erythrokeratoderma Variabilis without Connexin 31 or Connexin 30.3 Gene Mutation: Immunohistological, Ultrastructural and Genetic Studies

By Arita Ken   Akiyama Masashi   Tsuji Yukiko   Onozuka Takashi   Shimizu Hiroshi  

Acta Dermato-Venereologica, Vol. 83, Iss. 4, 2003-07 ,pp. : 266-270

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Connexin 26 (GJB2) Mutations in Two Swedish Patients with Atypical Vohwinkel (Mutilating Keratoderma plus Deafness) and KID Syndrome Both Extensively Treated with Acitretin

By Bondeson Marie-Louise   Nyström Anna-Maja   Gunnarsson Ulrika   Vahlquist Anders  

Acta Dermato-Venereologica, Vol. 86, Iss. 6, 2006-11 ,pp. : 503-508

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A Novel 5-bp Deletion Mutation in AAGAB Gene in a Chinese Family with Punctate Palmoplantar Keratoderma

By Li Ming   Dai Xunyi   Cheng Ruhong   Yang Lijia   Yao Zhirong   Liu Jiangbo  

Acta Dermato-Venereologica, Vol. 94, Iss. 3, 2014-05 ,pp. : 339-340

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A de Novo Mutation in the Keratin 9 Gene in a Family with Epidermolytic Palmoplantar Keratoderma from Northern Sweden

By Wennerstrand Lena   Häggbom Klingberg Melker   Hofer Per-Åke   Lundström Anita   Lind Lisbet  

Acta Dermato-Venereologica, Vol. 83, Iss. 2, 2003-01 ,pp. : 135-140

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