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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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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.
פורמט: Artigo
שפה:Inglês
יצא לאור: American Society of Hematology 2013
נושאים:
גישה מקוונת: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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