A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia Vicenza

J Thromb Haemost. 2005 Mar;3(3):600-1. doi: 10.1111/j.1538-7836.2005.01199.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Blood Coagulation Disorders, Inherited / genetics*
  • Coagulation Protein Disorders / genetics
  • Fibrinogen / chemistry
  • Fibrinogen / genetics*
  • Fibrinogens, Abnormal / genetics
  • Humans
  • Mutation, Missense*

Substances

  • Fibrinogens, Abnormal
  • fibrinogen Vicenza
  • fibrinopeptides gamma
  • Fibrinogen