Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding

Blood Coagul Fibrinolysis. 2015 Mar;26(2):231-2. doi: 10.1097/MBC.0000000000000196.
No abstract available

Publication types

  • Letter

MeSH terms

  • Afibrinogenemia / blood*
  • Afibrinogenemia / genetics*
  • Female
  • Hemorrhage / genetics*
  • Heterozygote
  • Humans
  • Male
  • Mutation*