The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect
- 1 June 1985
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 8 (S2), 135-136
- https://doi.org/10.1007/bf01811496
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with a Lipid-Storage Myopathy and Secondary Carnitine DeficiencyNew England Journal of Medicine, 1984
- Riboflavin‐responsive ethylmalonic—adipic aciduriaJournal of Inherited Metabolic Disease, 1984
- Glutaric aciduria type II: Biochemical investigation and treatment of a child diagnosed prenatallyJournal of Inherited Metabolic Disease, 1983
- Ethylmalonic-Adipic AciduriaJournal of Clinical Investigation, 1979