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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Bibliographic Details
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.
Format: Artigo
Language:Inglês
Published: American Society of Hematology 2013
Subjects:
Thrombosis and Hemostasis
Online Access: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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