Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations

BACKGROUND: Hemophilia A (HA) is an X-linked bleeding disorder caused by a deficiency in factor VIII (FVIII). von Willebrand disease (VWD) is characterized by a quantitative or qualitative defect in von Willebrand Factor (VWF). Patients with VWD with severely low VWF or VWD Type 2N (VWD2N), a VWD su...

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Detaylı Bibliyografya
Yayımlandı:J Thromb Haemost
Asıl Yazarlar: Boylan, Brian, Rice, Anne S., De Staercke, Christine, Eyster, M. Elaine, Yaish, Hassan M., Knoll, Christine M., Bean, Christopher J., Miller, Connie H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4512234/
https://ncbi.nlm.nih.gov/pubmed/25780857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jth.12902
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