Laboratory characterization of obligate carriers of type 3 von Willebrand disease with a potential role for Platelet Function Analyzer (PFA‐200)
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DOI: 10.1111/ijlh.13787
Abstract: Type 3 von Willebrand disease (VWD) is a rare autosomal recessive disorder characterized by undetectable von Willebrand Antigen (VWF:Ag). Carriers of type 3 VWD carry one null allele and have von Willebrand factor (VWF) at… read more here.
Keywords: willebrand; willebrand disease; von willebrand; role platelet ... See more keywords