Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical course
- 1 March 1996
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 19 (2) , 173-176
- https://doi.org/10.1007/bf01799422
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblastsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1993
- Systemic carnitine deficiency: Benefit of oral carnitine supplements vs. persisting biochemical abnormalitiesEuropean Journal of Pediatrics, 1984
- An improved and simplified radioisotopic assay for the determination of free and esterified carnitineJournal of Lipid Research, 1976