Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family

Thromb Haemost. 1998 Dec;80(6):1027-8.
No abstract available

Publication types

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

MeSH terms

  • 3' Untranslated Regions / genetics*
  • Abortion, Habitual / etiology
  • Adult
  • Aged
  • Amino Acid Substitution
  • Female
  • France
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Middle Aged
  • Oxidoreductases Acting on CH-NH Group Donors / genetics
  • Pedigree
  • Point Mutation*
  • Pregnancy
  • Prothrombin / genetics*
  • Pulmonary Embolism / epidemiology
  • Pulmonary Embolism / etiology*
  • Pulmonary Embolism / genetics
  • Risk Factors
  • Thrombophilia / genetics*
  • Thrombophlebitis / epidemiology
  • Thrombophlebitis / etiology*
  • Thrombophlebitis / genetics

Substances

  • 3' Untranslated Regions
  • Prothrombin
  • Oxidoreductases Acting on CH-NH Group Donors
  • Methylenetetrahydrofolate Reductase (NADPH2)