Gene symbol: F2. Disease: Hypoprothrombinemia

Hum Genet. 2005 May;116(6):543.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Humans
  • Hypoprothrombinemias
  • Mutation, Missense*
  • Prothrombin / genetics*

Substances

  • Prothrombin