The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles
Author:
Affiliation:
1. Department of Pathology and Molecular Medicine; Queen's University; Kingston ON Canada
2. Division of Hematology/Oncology; The Hospital for Sick Children; Toronto Ontario Canada
3. Department of Medicine; Queen's University; Kingston ON Canada
Funder
Canadian Hemophilia Society Research Grant
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12130/fullpdf
Reference37 articles.
1. The prevalence of symptomatic von Willebrand disease in primary care practice;Bowman;J Thromb Haemost,2010
2. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology;Eikenboom;Best Pract Res Clin Haematol,2001
3. Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study;Castaman;J Thromb Haemost,2006
4. When it comes to von Willebrand disease, does 1 + 1 = 3?;Montgomery;J Thromb Haemost,2006
5. An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease;Cumming;Thromb Haemost,2006
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