טוען...
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: | , , , , , , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society of Hematology
2013
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| 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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