Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene

Br J Haematol. 2002 Oct;119(1):282-3. doi: 10.1046/j.1365-2141.2002.377910.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Afibrinogenemia / congenital*
  • Afibrinogenemia / genetics
  • Female
  • Fibrinogen / genetics*
  • Hemorrhagic Disorders / genetics*
  • Homozygote
  • Humans
  • Infant, Newborn
  • Mutation / genetics*

Substances

  • fibrinogen Aalpha
  • Fibrinogen