Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival

Type 1 von Willebrand disease (VWD) is characterized by a partial quantitative deficiency of von Willebrand factor (VWF). Few VWF gene mutations have been identified that cause dominant type 1 VWD. The decreased survival of VWF in plasma has recently been identified as a novel mechanism for type 1 V...

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Bibliografiset tiedot
Päätekijät: Haberichter, Sandra L., Balistreri, Michael, Christopherson, Pamela, Morateck, Patricia, Gavazova, Stefana, Bellissimo, Daniel B., Manco-Johnson, Marilyn J., Gill, Joan Cox, Montgomery, Robert R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The American Society of Hematology 2006
Aiheet:
Hemostasis, Thrombosis, and Vascular Biology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895439/
https://ncbi.nlm.nih.gov/pubmed/16835381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2006-04-015065
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