3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: A coupled enzyme assay useful for their detection
- 1 September 1989
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 184 (1) , 57-64
- https://doi.org/10.1016/0009-8981(89)90256-8
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria.Journal of Clinical Investigation, 1986
- The analysis of acyl-Coenzyme A derivatives by reverse-phase high-performance liquid chromatographyAnalytical Biochemistry, 1983
- Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolismThe Journal of Pediatrics, 1982
- Deficiency of propionyl-CoA carboxylase and methylcrotonyl-CoA carboxylase in a patient with methylcrotonylglycinuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1977