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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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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: 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.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: American Society of Hematology 2013
Θέματα:
Διαθέσιμο Online: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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