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A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome.
Trizuljak, Jakub; Kozubík, Katerina Stano; Radová, Lenka; Pesová, Michaela; Pál, Karol; Réblová, Kamila; Stehlíková, Olga; Smejkal, Petr; Zavrelová, Jirina; Pacejka, Milan; Mayer, Jirí; Pospísilová, Sárka; Doubek, Michael.
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  • Trizuljak J; a Department of Internal Medicine- Hematology and Oncology, University Hospital Brno and Faculty of Medicine , Masaryk University , Brno , Czech Republic.
  • Kozubík KS; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Radová L; a Department of Internal Medicine- Hematology and Oncology, University Hospital Brno and Faculty of Medicine , Masaryk University , Brno , Czech Republic.
  • Pesová M; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Pál K; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Réblová K; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Stehlíková O; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Smejkal P; b Central European Institute of Technology , Masaryk University , Brno , Czech Republic.
  • Zavrelová J; a Department of Internal Medicine- Hematology and Oncology, University Hospital Brno and Faculty of Medicine , Masaryk University , Brno , Czech Republic.
  • Pacejka M; c Department of Clinical Hematology , University Hospital Brno , Brno , Czech Republic.
  • Mayer J; d Department of Laboratory Methods, Faculty of Medicine , Masaryk University , Brno , Czech Republic.
  • Pospísilová S; c Department of Clinical Hematology , University Hospital Brno , Brno , Czech Republic.
  • Doubek M; d Department of Laboratory Methods, Faculty of Medicine , Masaryk University , Brno , Czech Republic.
Platelets ; 29(8): 827-833, 2018 Dec.
Article en En | MEDLINE | ID: mdl-30332551
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Bernard-Soulier / Mutación Puntual / Complejo GPIb-IX de Glicoproteína Plaquetaria Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Platelets Asunto de la revista: HEMATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: República Checa
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Bernard-Soulier / Mutación Puntual / Complejo GPIb-IX de Glicoproteína Plaquetaria Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Platelets Asunto de la revista: HEMATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: República Checa