Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review.

Diociaiuti, A; Castiglia, D; Naim, M; Condorelli, A G; Zambruno, G; El Hachem, M

Diociaiuti, A; Castiglia, D; Naim, M; Condorelli, A G; Zambruno, G; El Hachem, M.

Afiliación

Diociaiuti A; Dermatology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Castiglia D; Laboratory of Molecular and Cell Biology, Istituto Dermopatico dell'Immacolata, IRCCS, Rome, Italy.
Naim M; Dermatology Section, Shifa Hospital, Gaza, State of Palestine.
Condorelli AG; Genetic and Rare Diseases Research Area, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Zambruno G; Genetic and Rare Diseases Research Area, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
El Hachem M; Dermatology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

J Eur Acad Dermatol Venereol ; 32(4): e149-e151, 2018 Apr.

Article en En | MEDLINE | ID: mdl-29024068

Asunto(s)

Epidermólisis Ampollosa Simple/genética; Queratina-14/genética; Mutación; Adolescente; Adulto; Árabes/genética; Femenino; Humanos; Masculino; Linaje; Adulto Joven

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epidermólisis Ampollosa Simple / Queratina-14 / Mutación Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2018 Tipo del documento: Article País de afiliación: Italia

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