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Afibrinogenemia with two compound heterozygous mutations in FGA gene.
Feugray, Guillaume; Billoir, Paul; Casini, Alessandro; Neerman-Arbez, M; Barbay, Virginie; Chamouni, Pierre; Schneider, Pascale; Le Cam Duchez, Véronique.
Afiliação
  • Feugray G; UNIROUEN, INSERM U1096, Vascular Hemostasis Unit, Normandie University, Rouen University Hospital, France.
  • Billoir P; UNIROUEN, INSERM U1096, Vascular Hemostasis Unit, Normandie University, Rouen University Hospital, France.
  • Casini A; Division of Angiology and Hemostasis, Faculty of Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Neerman-Arbez M; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Barbay V; UNIROUEN, INSERM U1096, Vascular Hemostasis Unit, Normandie University, Rouen University Hospital, France.
  • Chamouni P; Hemophilia Care Center, Rouen University Hospital, Rouen, France.
  • Schneider P; Hemophilia Care Center, Rouen University Hospital, Rouen, France.
  • Le Cam Duchez V; Department of Pediatric Hematology and Oncology, Rouen University Hospital, Rouen, France.
Haemophilia ; 27(5): e641-e644, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34255402
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Afibrinogenemia Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Afibrinogenemia Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article