Associated Papers
Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD.
Flood VH et al.
Journal of Thrombosis and Haemostasis : Jth, 2010
von Willebrand factor A1 domain can adequately substitute for A3 domain in recruitment of flowing platelets to collagen.
Bonnefoy A et al.
Journal of Thrombosis and Haemostasis : Jth, 2006
Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency.
Casaña P et al.
Haematologica, 2006
Von Willebrand factor and von Willebrand disease.
Budde U et al.
Reviews in Clinical and Experimental Hematology, 2001
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