A defect in l-isoleucine metabolism associated with α-methyl-β-hydroxybutyric and α-methylacetoacetic aciduria: Quantitative in vivo and in vitro studies
Authors:
- 17 December 1974
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta
- Vol. 57 (3) , 269-281
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemiasBiochemical Medicine, 1974
- An Inherited Disorder of Isoleucine Catabolism Causing Accumulation of α-Methylacetoacetate and α-Methyl-β-hydroxybutyrate, and Intermittent Metabolic AcidosisPediatric Research, 1973
- The gas-chromatographic diagnosis of intermittent maple syrup urine disease (branch-chain ketoaciduria)Clinica Chimica Acta, 1972
- The identification of tiglylglycine in the urine of a child with β-methylcrotonylgeycinuriaClinica Chimica Acta, 1972
- A " NEW " DISORDER OF ISOLEUCINE CATABOLISMThe Lancet, 1971