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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society of Hematology 2013
Ämnen:
Thrombosis and Hemostasis
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk