Severe thrombophilia in a paediatric patient with end-stage renal disease: detection of the prothrombin gene G20210A mutation

Nephrol Dial Transplant. 1998 Aug;13(8):2130-2. doi: 10.1093/ndt/13.8.2130.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Female
  • Humans
  • Kidney Failure, Chronic / complications*
  • Kidney Failure, Chronic / therapy
  • Kidney Transplantation
  • Mutation* / genetics
  • Prothrombin / genetics*
  • Renal Dialysis
  • Thrombophilia / etiology*
  • Thrombophilia / genetics*

Substances

  • Prothrombin