Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism
- 1 August 1984
- journal article
- research article
- Published by Elsevier BV in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 141 (2-3), 227-234
- https://doi.org/10.1016/0009-8981(84)90014-7
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Linear relationship between the R- and S-enantiomers of β-aminoisobutyric acid in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- The activities of thymidine metabolising enzymes during the cell cycle of a human lymphocyte cell line LAZ-007 synchronised by centrifugal elutriationBiochimica et Biophysica Acta (BBA) - General Subjects, 1980
- Urinary purines and pyrimidines in patients with hyperammonemia of various originsClinica Chimica Acta; International Journal of Clinical Chemistry, 1980
- Gas chromatography of urinary N-phenylacetylglutamineJournal of Chromatography B: Biomedical Sciences and Applications, 1979
- Two-dimensional thin-layer chromatography for the screening of disorders of purine and pyrimidine metabolismClinica Chimica Acta; International Journal of Clinical Chemistry, 1978