Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation

Thromb Haemost. 2011 Jun;105(6):1120-3. doi: 10.1160/TH10-11-0767. Epub 2011 Apr 20.
No abstract available

Publication types

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

MeSH terms

  • Child, Preschool
  • Consanguinity
  • DNA Mutational Analysis
  • Disease Progression
  • Factor V / genetics
  • Factor V / immunology
  • Factor V / metabolism*
  • Factor V Deficiency / diagnosis*
  • Factor V Deficiency / epidemiology
  • Factor V Deficiency / genetics*
  • Factor V Deficiency / physiopathology
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Testing
  • Hemorrhage
  • Humans
  • India
  • Infant
  • Male
  • Mutation / genetics
  • Population Groups*
  • Prognosis

Substances

  • Factor V