Characterisation of a novel nonsense mutation in FGG (Fibrinogen Poznan) causing hypofibrinogenaemia with a mild bleeding tendency

Thromb Haemost. 2010 Mar;103(3):677-9. doi: 10.1160/TH09-06-0390. Epub 2010 Feb 2.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Afibrinogenemia / genetics*
  • Afibrinogenemia / pathology
  • Codon, Nonsense*
  • Fibrinogens, Abnormal / genetics*
  • Hemorrhagic Disorders / genetics
  • Humans
  • Male
  • Pedigree

Substances

  • Codon, Nonsense
  • Fibrinogens, Abnormal