Correction of a dominant-negative von Willebrand factor multimerization defect by small interfering RNA-mediated allele-specific inhibition of mutant von Willebrand factor
Author:
Affiliation:
1. Department of Internal Medicine (Thrombosis and Hemostasis); Einthoven Laboratory for Vascular and Regenerative Medicine; Leiden University Medical Center; Leiden the Netherlands
Funder
Landsteiner Foundation for Blood transfusion Research
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.14140/fullpdf
Reference37 articles.
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2. The genetic basis of von Willebrand disease;Goodeve;Blood Rev,2010
3. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor;Sadler;J Thromb Haemost,2006
4. Treatment of von Willebrand disease;Curnow;Semin Thromb Hemost,2016
5. 1-Deamino-8-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands’ diseases;Mannucci;Lancet,1977
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