Common genomic sequence variation of the prothrombin gene and risk of non-fatal myocardial infarction in white women

J Thromb Haemost. 2005 Dec;3(12):2809-11. doi: 10.1111/j.1538-7836.2005.01641.x.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Female
  • Genetic Variation
  • Humans
  • Myocardial Infarction / ethnology
  • Myocardial Infarction / genetics*
  • Myocardial Infarction / mortality
  • Prothrombin / genetics*
  • Risk Factors
  • White People

Substances

  • Prothrombin