The enzymes of mitochondrial fatty acid oxidation
- 31 May 1994
- journal article
- review article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 226 (2) , 211-224
- https://doi.org/10.1016/0009-8981(94)90216-x
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- A Novel Disease with Deficiency of Mitochondrial Very-Long-Chain Acyl-CoA DehydrogenaseBiochemical and Biophysical Research Communications, 1993
- A fatal neonatal case of medium-chain acyl-coenzyme a dehydrogenase deficiency with homozygous A→G985 transitionThe Journal of Pediatrics, 1992
- Fatty acid oxidation disorders: A new class of metabolic diseasesThe Journal of Pediatrics, 1992
- Beta-oxidation of long-chain fatty acids by human fibroblasts: Evidence for a novel long-chain acyl-coenzyme a dehydrogenaseBiochemical and Biophysical Research Communications, 1992
- Structural and functional features of different types of cytoplasmic fatty acid-binding proteinsBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
- Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyBiochemical and Biophysical Research Communications, 1990
- Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidationJournal of Inherited Metabolic Disease, 1990
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromesThe Journal of Pediatrics, 1986
- Muscle Carnitine Palmityltransferase Deficiency and MyoglobinuriaScience, 1973