Stroke in an infant heterozygous carrier of both Factor V G1691A and the G20210A prothrombin mutation

Thromb Haemost. 2003 Oct;90(4):760-3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brain Ischemia / diagnosis
  • Brain Ischemia / genetics
  • Factor V / genetics*
  • Family Health
  • Heterozygote
  • Humans
  • Infant
  • Male
  • Point Mutation*
  • Prothrombin / genetics*
  • Stroke / diagnosis
  • Stroke / genetics*
  • Thrombophilia / genetics

Substances

  • Factor V
  • Prothrombin