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. doi: 10.1111/j.1538-7836.2010.03869.x. Epub 2010 Mar 23.
No abstract available

Publication types

  • Letter

MeSH terms

  • Cell Line
  • Collagen / metabolism*
  • Humans
  • Mutation*
  • Protein Binding
  • von Willebrand Diseases / diagnosis*
  • von Willebrand Diseases / genetics
  • von Willebrand Diseases / metabolism
  • von Willebrand Factor / genetics*

Substances

  • von Willebrand Factor
  • Collagen