Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population

Thromb Res. 2020 May:189:39-41. doi: 10.1016/j.thromres.2020.02.025. Epub 2020 Mar 2.
No abstract available

Keywords: Antithrombin; Antithrombin deficiency; Coagulation inhibitor; SERPINC1; Thromboembolism.

Publication types

  • Letter

MeSH terms

  • Antithrombin III / genetics
  • Antithrombin III Deficiency* / genetics
  • Czech Republic / epidemiology
  • Humans
  • Mutation

Substances

  • SERPINC1 protein, human
  • Antithrombin III