Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene

Thromb Haemost. 1999 Oct;82(4):1366-7.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Budd-Chiari Syndrome / genetics*
  • Child
  • Factor V / genetics*
  • Female
  • Heterozygote
  • Humans
  • Mutation
  • Prothrombin / genetics*

Substances

  • factor V Leiden
  • Factor V
  • Prothrombin