Case Report: Uncommon Association of <i>ITGB4</i> and <i>KRT10</i> Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita.

Matyas, Melinda; Miclea, Diana; Zaharie, Gabriela

Case Report: Uncommon Association of ITGB4 and KRT10 Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita.

Matyas, Melinda; Miclea, Diana; Zaharie, Gabriela.

Afiliação

Matyas M; Neonatology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Miclea D; Genetics, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Zaharie G; Neonatology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Front Genet ; 12: 641977, 2021.

Article em En | MEDLINE | ID: mdl-34306001

Palavras-chave

DNA sequencing; aplasia cutis; epidermolysis bullosa; newborn; pyloric atresia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Romênia

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