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Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5.
Kumagai, Y; Umegaki-Arao, N; Sasaki, T; Nakamura, Y; Takahashi, H; Ashida, A; Tsunemi, Y; Kawashima, M; Shimizu, A; Ishiko, A; Nakamura, K; Tsuchihashi, H; Amagai, M; Kubo, A.
Afiliación
  • Kumagai Y; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
  • Umegaki-Arao N; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
  • Sasaki T; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
  • Nakamura Y; KOSE Endowed Program for Skin Care and Allergy Prevention, Keio University School of Medicine, Tokyo, Japan.
  • Takahashi H; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
  • Ashida A; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
  • Tsunemi Y; Department of Dermatology, Shinshu University School of Medicine, Nagano, Japan.
  • Kawashima M; Department of Dermatology, Tokyo Women's Medical University, Tokyo, Japan.
  • Shimizu A; Department of Dermatology, Tokyo Women's Medical University, Tokyo, Japan.
  • Ishiko A; Department of Dermatology, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan.
  • Nakamura K; Department of Dermatology, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan.
  • Tsuchihashi H; Department of Dermatology, Saitama Medical University, Saitama, Japan.
  • Amagai M; Department of Dermatology, Saitama Medical University, Saitama, Japan.
  • Kubo A; Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
J Eur Acad Dermatol Venereol ; 31(5): e241-e243, 2017 May.
Article en En | MEDLINE | ID: mdl-27730678
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Epidermólisis Ampollosa Simple / Mutación del Sistema de Lectura / Eritema / Queratina-5 Tipo de estudio: Diagnostic_studies Límite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2017 Tipo del documento: Article País de afiliación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Epidermólisis Ampollosa Simple / Mutación del Sistema de Lectura / Eritema / Queratina-5 Tipo de estudio: Diagnostic_studies Límite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2017 Tipo del documento: Article País de afiliación: Japón