Clinical significance of two mutations in the factor IX gene in a family with haemophilia B

Haemophilia. 2010 Mar;16(2):374-6. doi: 10.1111/j.1365-2516.2009.02143.x. Epub 2009 Nov 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • DNA Mutational Analysis
  • Exons / genetics
  • Factor IX / genetics*
  • Female
  • Genetic Testing
  • Hemophilia B / genetics*
  • Humans
  • Male
  • Mutation*

Substances

  • Factor IX