Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene--a case report

Haemophilia. 2013 Sep;19(5):e310-3. doi: 10.1111/hae.12190. Epub 2013 May 28.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, X*
  • Factor VIII / genetics*
  • Female
  • Hemophilia A / genetics*
  • Humans
  • Mutation, Missense*

Substances

  • Factor VIII