Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts
- 22 January 1993
- journal article
- case report
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1180 (3) , 327-329
- https://doi.org/10.1016/0925-4439(93)90058-9
Abstract
No abstract availableKeywords
This publication has 2 references indexed in Scilit:
- Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase.Published by Elsevier ,2021
- Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblastsClinica Chimica Acta; International Journal of Clinical Chemistry, 1992