Type 2B von Willebrand disease in seven individuals from three different families: phenotypic and genotypic characterization

Thromb Haemost. 2007 Jul;98(1):251-4.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Dimerization
  • Family Health
  • Genotype
  • Hemorrhage / etiology
  • Humans
  • Middle Aged
  • Mutation, Missense*
  • Phenotype
  • Thrombocytopenia / etiology
  • von Willebrand Diseases / genetics*
  • von Willebrand Diseases / pathology*
  • von Willebrand Factor / genetics

Substances

  • von Willebrand Factor