Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10.

Abdul-Wahab, A; Takeichi, T; Liu, L; Stephens, C; Akiyama, M; McGrath, J A

Abdul-Wahab, A; Takeichi, T; Liu, L; Stephens, C; Akiyama, M; McGrath, J A.

Afiliación

Abdul-Wahab A; St John's Institute of Dermatology, King's College London (Guy's Campus), London, UK.
Takeichi T; St John's Institute of Dermatology, King's College London (Guy's Campus), London, UK.
Liu L; Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Stephens C; Viapath, St Thomas' Hospital, London, UK.
Akiyama M; Department of Dermatology, Poole Hospital NHS Foundation Trust, Poole, UK.
McGrath JA; Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Clin Exp Dermatol ; 41(3): 290-3, 2016 Apr.

Article en En | MEDLINE | ID: mdl-26338057

Asunto(s)

Hiperqueratosis Epidermolítica/genética; Queratina-10/genética; Mutación Missense; Adulto; Femenino; Humanos; Lactante; Masculino; Persona de Mediana Edad; Linaje

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Hiperqueratosis Epidermolítica / Mutación Missense / Queratina-10 Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Clin Exp Dermatol Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google