Article
[Molecular study of type 2 von Willebrand disease].
Casopis lekaru ceskych - 1 Jan 2003
Habart D, Smejkal P, Matýsková M, Turek P, Hrachovinová I, Vorlová Z
Abstract excerpt
BACKGROUND: von Willebrand disease is an inherited bleeding disorders caused by mutations in the von Willebrand factor gene. We attempted to characterise the phenotype and the genotype in the first five families in Czech Republic affected by this heterogeneous disorder. METHODS AND RESULTS: The level of FVIII was measured by the one stage assay, the vWF:Ag by the immunoelectrophoresis, vWF:RiCo by aggregometry....
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