Muscle cytochrome c oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl‐CoA dehydrogenase deficiency
- 1 May 1993
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 16 (3) , 553-556
- https://doi.org/10.1007/bf00711679
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Cytochrome c Oxidase DeficiencyPediatric Research, 1990
- Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathyJournal of the Neurological Sciences, 1987
- Urinary excretion of succinylacetone and δ-aminolevulinic acid in patients with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type IIJournal of Inherited Metabolic Disease, 1980
- Ethylmalonic-Adipic AciduriaJournal of Clinical Investigation, 1979
- An improved and simplified radioisotopic assay for the determination of free and esterified carnitineJournal of Lipid Research, 1976
- A MICROSPECTROPHOTOMETRIC METHOD FOR THE DETERMINATION OF CYTOCHROME OXIDASEJournal of Biological Chemistry, 1951