Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD. J Thromb Haemost 2010 Jun;8(6):1431-3
Date
03/30/2010Pubmed ID
20345715Pubmed Central ID
PMC3892206DOI
10.1111/j.1538-7836.2010.03869.xScopus ID
2-s2.0-77954496769 (requires institutional sign-in at Scopus site) 82 CitationsAuthor List
Flood VH, Lederman CA, Wren JS, Christopherson PA, Friedman KD, Hoffmann RG, Montgomery RRAuthors
Veronica H. Flood MD Chief, Professor in the Pediatrics department at Medical College of WisconsinKenneth D. Friedman MD Professor in the Medicine department at Medical College of Wisconsin
Robert R. Montgomery MD Emeritus Professor in the Pediatrics department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
Cell LineCollagen
Humans
Mutation
Protein Binding
von Willebrand Diseases
von Willebrand Factor
