Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency

Haemophilia. 2012 Mar;18(2):e51-3. doi: 10.1111/j.1365-2516.2011.02747.x. Epub 2012 Jan 18.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • DNA Mutational Analysis
  • Factor V / chemistry
  • Factor V / genetics*
  • Factor V Deficiency / genetics*
  • Humans
  • Male
  • Mutation*
  • Mutation, Missense
  • RNA Splice Sites / genetics

Substances

  • RNA Splice Sites
  • Factor V