Eclampsia in a woman homozygous for the prothrombin G20210A mutation

Thromb Haemost. 2004 Jan;91(1):201-2.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Eclampsia / genetics*
  • Female
  • HELLP Syndrome / genetics*
  • Homozygote
  • Humans
  • Mutation*
  • Pregnancy
  • Pregnancy Complications, Hematologic
  • Prothrombin / genetics*
  • Time Factors

Substances

  • Prothrombin