The allopurinol loading test in detecting obligate heterozygotes for OCT deficiency
- 1 January 1994
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 17 (1) , 133-134
- https://doi.org/10.1007/bf00735417
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- The allopurinol loading test for identification of carriers for ornithine carbamoyl transferase deficiency: studies in a healthy control population and females at riskClinica Chimica Acta; International Journal of Clinical Chemistry, 1994
- Allopurinol challenge test in childrenJournal of Inherited Metabolic Disease, 1991
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- Allopurinol-Induced OrotidinuriaNew England Journal of Medicine, 1990