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ABSTRACT: Summary
Background A novel variant, p.Pro2808Leufs*24, in the von Willebrand factor (VWF) gene was previously identified in the Canadian von Willebrand disease (VWD) patient population. Clinical observations of type 3 VWD patients with this variant indicate a milder bleeding phenotype compared with other type 3 patients. Objective To assess the effect of the Pro2808Leufs*24 variant on the molecular pathogenesis of VWD and correlate this with
SUBMITTER: Bowman ML
PROVIDER: S-EPMC5949882 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature