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A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma.
Khabou, Boudour; Trigui, Ayman; Boudawara, Tahya Sellami; Keskes, Leila; Kamoun, Hassen; Barbu, Véronique; Fakhfakh, Faiza.
Afiliação
  • Khabou B; Laboratory of Molecular and Functional Genetics, Faculty of Science, University of Sfax, Tunisia. Electronic address: Boudour.khabou.bio@gmail.com.
  • Trigui A; Department of General Surgery, Habib Bourguiba Hospital, 3027 Sfax, Tunisia.
  • Boudawara TS; Anatomo Pathology's Department, Habib Bourguiba Hospital, Sfax, Tunisia.
  • Keskes L; Laboratory of Molecular and Human Genetics, Faculty of Medecine, University of Sfax, Tunisia.
  • Kamoun H; Laboratory of Molecular and Human Genetics, Faculty of Medecine, University of Sfax, Tunisia.
  • Barbu V; Sorbonne University Medical School, APHP, St Antoine Hospital, Medical Biology and Pathology Department, LCBGM, 75012 Paris, France.
  • Fakhfakh F; Laboratory of Molecular and Functional Genetics, Faculty of Science, University of Sfax, Tunisia.
Clin Chim Acta ; 495: 598-605, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31181191
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Colelitíase / Colangiocarcinoma / Subfamília B de Transportador de Cassetes de Ligação de ATP / Homozigoto Tipo de estudo: Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Colelitíase / Colangiocarcinoma / Subfamília B de Transportador de Cassetes de Ligação de ATP / Homozigoto Tipo de estudo: Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2019 Tipo de documento: Article