Genotype/phenotype association in von Willebrand disease: is the glass half full or empty?
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2009.03367.x/fullpdf
Reference25 articles.
1. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor;Sadler;J Thromb Haemost,2006
2. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology;Eikenboom;Best Pract Res Clin Haematol,2001
3. 3ISTH SSC VWF Database. 2008; http://www.vwf.group.shef.ac.uk/. Accessed 23 January 2009.
4. A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3;Schneppenheim;J Thromb Haemost,2007
5. Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands;Zhang;Proc Natl Acad Sci USA,1993
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