Dihydropyrimidinuria without clinical symptoms

J Inherit Metab Dis. 1996;19(5):701-2. doi: 10.1007/BF01799851.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Amidohydrolases / deficiency
  • Chromatography, High Pressure Liquid
  • Female
  • Humans
  • Infant
  • Male
  • Mass Screening
  • Purine-Pyrimidine Metabolism, Inborn Errors / diagnosis
  • Purine-Pyrimidine Metabolism, Inborn Errors / metabolism*
  • Pyrimidines / urine*

Substances

  • Pyrimidines
  • Amidohydrolases
  • dihydropyrimidinase