No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation

The diagnosis of von Willebrand disease (VWD) is complicated by issues with current laboratory testing, particularly the ristocetin cofactor activity assay (VWF:RCo). We have recently reported a sequence variation in the von Willebrand factor (VWF) A1 domain, p.D1472H (D1472H), associated with a dec...

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Detalhes bibliográficos
Main Authors: Flood, Veronica H., Friedman, Kenneth D., Gill, Joan Cox, Haberichter, Sandra L., Christopherson, Pamela A., Branchford, Brian R., Hoffmann, Raymond G., Abshire, Thomas C., Dunn, Amy L., Di Paola, Jorge A., Hoots, W. Keith, Brown, Deborah L., Leissinger, Cindy, Lusher, Jeanne M., Ragni, Margaret V., Shapiro, Amy D., Montgomery, Robert R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2013
Assuntos:
Thrombosis and Hemostasis
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3643771/
https://ncbi.nlm.nih.gov/pubmed/23520336
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2012-12-471672
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