Dihydropyrimidine dehydrogenase deficiency — A further case
- 1 June 1985
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 8 (S2) , 115-116
- https://doi.org/10.1007/bf01811485
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- 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
- 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 excretion of thymine and uracil in a two-year-old child with a malignant tumor of the brain.Clinical Chemistry, 1979