Identification of a novel candidate splice site mutation (0874 + 1G > A) in a type 3 von Willebrand disease patient

Thromb Haemost. 2007 Aug;98(2):464-6.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • DNA Mutational Analysis
  • Humans
  • Male
  • Mutation*
  • Phenotype
  • RNA Splice Sites / genetics*
  • von Willebrand Diseases / genetics*
  • von Willebrand Factor / genetics*

Substances

  • RNA Splice Sites
  • von Willebrand Factor