Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia

Eur J Haematol. 2008 Jan;80(1):87-9. doi: 10.1111/j.1600-0609.2007.00965.x. Epub 2007 Nov 19.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Factor IX / genetics
  • Hemophilia B / complications
  • Hemophilia B / diagnosis
  • Hemophilia B / genetics*
  • Hemorrhage / genetics
  • Humans
  • Mutation
  • Phenotype
  • Thrombophilia / complications
  • Thrombophilia / diagnosis
  • Thrombophilia / genetics*

Substances

  • Factor IX