Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families

Haemophilia. 2015 Nov;21(6):e519-23. doi: 10.1111/hae.12788. Epub 2015 Aug 17.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Afibrinogenemia / diagnosis
  • Afibrinogenemia / genetics*
  • Asian People
  • Child
  • Child, Preschool
  • Female
  • Fibrinogen / genetics*
  • Fibrinogen / metabolism
  • Humans
  • Infant
  • Male
  • Mutation

Substances

  • Fibrinogen