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.

Afiliação

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 em En | MEDLINE | ID: mdl-29024068

Assuntos

Epidermólise Bolhosa Simples/genética; Queratina-14/genética; Mutação; Adolescente; Adulto; Árabes/genética; Feminino; Humanos; Masculino; Linhagem; Adulto Jovem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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