A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec

Haemophilia. 2024 May;30(3):858-861. doi: 10.1111/hae.15006. Epub 2024 Apr 1.
No abstract available

Publication types

  • Letter
  • Case Reports

MeSH terms

  • Adult
  • Afibrinogenemia* / genetics
  • Female
  • Fibrinogen* / genetics
  • Humans
  • Male
  • Mutation, Missense*
  • Pedigree*
  • Quebec

Substances

  • Fibrinogen
  • FGG protein, human