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Characterization of VWF gene conversions causing von Willebrand disease.
Ahmad, Firdos; Kannan, Meganathan; Obser, Tobias; Budde, Ulrich; Schneppenheim, Sonja; Saxena, Renu; Schneppenheim, Reinhard.
Afiliação
  • Ahmad F; Sharjah Institute for Medical Research and, College of Medicine, University of Sharjah, Sharjah, UAE.
  • Kannan M; Division of Blood and Vascular Biology, Department of Life Sciences, School of Basic and Applied Sciences, Central University of Tamilnadu, Thiruvarur, India.
  • Obser T; Department of Pediatric Haematology and Oncology, University Medical Centre, Eppendorf, Hamburg, Germany.
  • Budde U; Medilys Laboratory Coagulation, Asklepios Hospital Altona, Hamburg, Germany.
  • Schneppenheim S; Medilys Laboratory Coagulation, Asklepios Hospital Altona, Hamburg, Germany.
  • Saxena R; Department of Haematology, All India Institute of Medical Sciences, New Delhi, India.
  • Schneppenheim R; Department of Pediatric Haematology and Oncology, University Medical Centre, Eppendorf, Hamburg, Germany.
Br J Haematol ; 184(5): 817-825, 2019 03.
Article em En | MEDLINE | ID: mdl-30488424
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de von Willebrand / Fator de von Willebrand / Mutação de Sentido Incorreto Tipo de estudo: Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de von Willebrand / Fator de von Willebrand / Mutação de Sentido Incorreto Tipo de estudo: Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article