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Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism.

AuthorsM Duran, P Rovers, P K de Bree, C H Schreuder, H Beukenhorst, L Dorland, R Berger
JournalJournal of inherited metabolic disease (J Inherit Metab Dis) Vol. 14 Issue 3 Pg. 367-70 ( 1991) ISSN: 0141-8955 [Print] United States
PMID1770794 (Publication Type: Case Reports, Journal Article)
Chemical References
  • dihydrouracil
  • Uracil
  • Amidohydrolases
  • dihydropyrimidinase
  • Alanine
Topics
  • Alanine (urine)
  • Amidohydrolases (deficiency)
  • Chromatography, High Pressure Liquid
  • Fibroblasts (metabolism)
  • Humans
  • Infant
  • Liver (metabolism)
  • Male
  • Neutrophils (metabolism)
  • Purine-Pyrimidine Metabolism, Inborn Errors (urine)
  • Spectrophotometry, Ultraviolet
  • Uracil (analogs & derivatives, urine)

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