Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX

Haemophilia. 2021 Jul;27(4):e462-e465. doi: 10.1111/hae.14146. Epub 2020 Sep 30.
No abstract available

Publication types

  • Letter

MeSH terms

  • Factor IX / genetics
  • Factor VIII / genetics
  • Hemophilia A*
  • Hemophilia B* / genetics
  • Humans
  • Phenotype

Substances

  • Factor VIII
  • Factor IX