Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.
Open Access
- 1 December 1973
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 48 (12), 975-977
- https://doi.org/10.1136/adc.48.12.975
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- The gas-chromatographic diagnosis of intermittent maple syrup urine disease (branch-chain ketoaciduria)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation.1972
- BETA-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY: A NEW METABOLIC ERROR IN LEUCINE DEGRADATIONPediatrics, 1972
- The identification of tiglylglycine in the urine of a child with β-methylcrotonylgeycinuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIAThe Lancet, 1971
- $beta;-HYDROXYISOVALERIC ACIDURIA AND $beta;-METHYLCROTONYLGLYCINURIA: A NEW INBORN ERROR OF METABOLISMThe Lancet, 1970