Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis

Haemophilia. 2007 Mar;13(2):221-2. doi: 10.1111/j.1365-2516.2006.01432.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abortion, Habitual / genetics*
  • Adult
  • Factor XIII Deficiency / congenital
  • Factor XIII Deficiency / genetics*
  • Factor XIIIa / genetics*
  • Female
  • Humans
  • Mutation / genetics*
  • Pregnancy
  • Pregnancy Complications, Hematologic / genetics*
  • Pregnancy Outcome

Substances

  • Factor XIIIa