Article
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).
Blood - 1 Jan 2007
Goodeve Anne, Eikenboom Jeroen, Castaman Giancarlo, Rodeghiero Francesco, Federici Augusto B, Batlle Javier, Meyer Dominique, Mazurier Claudine, Goudemand Jenny, Schneppenheim Reinhard, Budde Ulrich, Ingerslev Jorgen, Habart David, Vorlova Zdena, Holmberg Lars, Lethagen Stefan, Pasi John, Hill Frank, Hashemi Soteh Mohammad, Baronciani Luciano, Hallden Christer, Guilliatt Andrea, Lester Will, Peake Ian
Abstract excerpt
Type 1 von Willebrand disease (VWD) is characterized by a personal and family history of bleeding coincident with reduced levels of normal plasma von Willebrand factor (VWF). The molecular basis of the disorder is poorly understood. The aims of this study were to determine phenotype and genotype...
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