Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion

Haemophilia. 2020 Jul;26(4):e194-e197. doi: 10.1111/hae.13974. Epub 2020 Mar 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Afibrinogenemia / blood
  • Afibrinogenemia / genetics*
  • Blood Coagulation / genetics
  • Fibrinogen / genetics*
  • Humans
  • Male
  • Middle Aged

Substances

  • FGB protein, human
  • FGG protein, human
  • Fibrinogen