Gly392Cys missense mutation in the A2 domain of factor V causing severe factor V deficiency: molecular characterization by expression of the recombinant protein

Thromb Haemost. 2005 Mar;93(3):614-5.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Cloning, Molecular
  • Factor V / genetics*
  • Factor V / metabolism
  • Factor V Deficiency / genetics*
  • Humans
  • Male
  • Mutation, Missense*
  • Pedigree

Substances

  • Factor V