Clinical and biochemical findings in six patients with pyrimidine degradation defects
- 1 January 1994
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 17 (1), 130-132
- https://doi.org/10.1007/bf00735416
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismClinica Chimica Acta; International Journal of Clinical Chemistry, 1984
- Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1984