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Rapid discrimination of the phenotypic variants of von Willebrand disease

Approximately 20% to 25% of patients with von Willebrand disease (VWD) have a qualitative defect of the von Willebrand factor (VWF) protein activities. Variant VWD typically is classified as type 1C, 2A, 2B, 2M, or 2N depending on the VWF activity defect. Traditionally, diagnosis has relied on multi...

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Bibliografische gegevens
Gepubliceerd in:Blood
Hoofdauteurs: Roberts, Jonathan C., Morateck, Patti A., Christopherson, Pamela A., Yan, Ke, Hoffmann, Raymond G., Gill, Joan Cox, Montgomery, Robert R.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Hematology 2016
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4874227/
https://ncbi.nlm.nih.gov/pubmed/26917779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-11-664680
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