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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
Casini, A; Vilar, R; Beauverd, Y; Aslan, D; Devreese, K; Mondelaers, V; Alberio, L; Gubert, C; de Moerloose, P; Neerman-Arbez, M.
Afiliación
  • Casini A; Division of Angiology and Haemostasis, Faculty of Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Vilar R; Department of Genetic Medicine and Development, University Medical School of Geneva, Geneva, Switzerland.
  • Beauverd Y; Haematology Division, Faculty of Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Aslan D; Pediatric Hematology Unit, Faculty of Medicine, Gazi University, Ankara, Turkey.
  • Devreese K; Coagulation Laboratory, Ghent University Hospital, Ghent, Belgium.
  • Mondelaers V; Department of Pediatric Hemato-oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
  • Alberio L; Service et Laboratoire central d'Hématologie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Gubert C; Department of Genetic Medicine and Development, University Medical School of Geneva, Geneva, Switzerland.
  • de Moerloose P; Division of Angiology and Haemostasis, Faculty of Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Neerman-Arbez M; Department of Genetic Medicine and Development, University Medical School of Geneva, Geneva, Switzerland.
Haemophilia ; 23(4): 583-589, 2017 Jul.
Article en En | MEDLINE | ID: mdl-28306188

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrinógeno / Afibrinogenemia / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrinógeno / Afibrinogenemia / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Suiza