Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and protein S deficiency. a family study

Haematologica. 2003 Jun;88(6):ECR20.
No abstract available

MeSH terms

  • Blood Coagulation Disorders, Inherited / complications*
  • Blood Coagulation Disorders, Inherited / genetics*
  • Factor V / genetics*
  • Family Health
  • Female
  • Humans
  • Male
  • Mutation*
  • Protein S Deficiency / complications*
  • Prothrombin / genetics*

Substances

  • factor V Leiden
  • Factor V
  • Prothrombin