Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidation
- 1 May 1990
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (3), 311-314
- https://doi.org/10.1007/bf01799383
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- The inborn errors of peroxisomal β‐oxidation: A reviewJournal of Inherited Metabolic Disease, 1989
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- The existence of an inner-membrane-bound, long acyl-chain-specific 3-hydroxyacyl-CoA dehydrogenase in mammalian mitochondriaBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1982
- Purification and properties of mitochondrial and peroxisomal 3-hydroxyacyl-CoA dehydrogenase from rat liverArchives of Biochemistry and Biophysics, 1980
- The Presence of a New 3‐Oxoacyl‐CoA Thiolase in Rat Liver PeroxisomesEuropean Journal of Biochemistry, 1980