Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD.

Authors :: Flood VH
Lederman CA
Wren JS
Christopherson PA
Friedman KD
Hoffmann RG
Montgomery RR
Source :: Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2010 Jun; Vol. 8 (6), pp. 1431-3. Date of Electronic Publication: 2010 Mar 23.
Publication Year :: 2010

Subjects :: Cell Line
Humans
Protein Binding
von Willebrand Diseases genetics
von Willebrand Diseases metabolism
Collagen metabolism
Mutation
von Willebrand Diseases diagnosis
von Willebrand Factor genetics

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