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

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Bibliographic Details
Published inJournal of thrombosis and haemostasis Vol. 8; no. 6; pp. 1431 - 1433
Main Authors FLOOD, V. H., LEDERMAN, C. A., WREN, J. S., CHRISTOPHERSON, P. A., FRIEDMAN, K. D., HOFFMANN, R. G., MONTGOMERY, R. R.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2010
Subjects
Cell Line
Collagen - metabolism
Humans
Mutation
Protein Binding
von Willebrand Diseases - diagnosis
von Willebrand Diseases - genetics
von Willebrand Diseases - metabolism
von Willebrand Factor - genetics
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:1538-7933
1538-7836
1538-7836
DOI:10.1111/j.1538-7836.2010.03869.x