Haemophilia B caused by mutation of a potential thrombin cleavage site in factor IX

Nucleic Acids Res. 1990 Mar 11;18(5):1310. doi: 10.1093/nar/18.5.1310.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Factor IX / genetics*
  • Factor IX / metabolism
  • Female
  • Hemophilia B / genetics*
  • Humans
  • Mutation*
  • Thrombin / metabolism*

Substances

  • Factor IX
  • Thrombin