Inherited disorders of straight chain fatty acid oxidation.
Open Access
- 1 January 1987
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 62 (1) , 6-7
- https://doi.org/10.1136/adc.62.1.6
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblastsBiochemical Medicine, 1985
- Riboflavin‐responsive ethylmalonic—adipic aciduriaJournal of Inherited Metabolic Disease, 1984
- General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesClinica Chimica Acta; International Journal of Clinical Chemistry, 1983