Fibrinogen Hangzhou: congenital dysfibrinogenemia caused by the novel missense mutation in FGG (γ308Asn→Thr)

Clin Chim Acta. 2014 Jan 20:428:106-9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Afibrinogenemia / genetics*
  • Asparagine / genetics*
  • China
  • Fibrinogen / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation, Missense / genetics*
  • Threonine / genetics*

Substances

  • Threonine
  • Asparagine
  • Fibrinogen

Supplementary concepts

  • Dysfibrinogenemia, Congenital