Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin alpha-helix D molecular pathology

Ann Hematol. 2005 Jan;84(1):56-8. doi: 10.1007/s00277-004-0906-3. Epub 2004 Aug 10.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Age of Onset
  • Antithrombin III / analysis
  • Antithrombin III / chemistry
  • Antithrombin III / genetics*
  • Antithrombin III Deficiency / complications
  • Antithrombin III Deficiency / diagnosis
  • Antithrombin III Deficiency / genetics*
  • Female
  • Humans
  • Mutation*
  • Thrombophilia / etiology
  • Thrombophilia / genetics*

Substances

  • Antithrombin III