Immunoreactive enzyme protein in medium-chain acyl-CoA dehydrogenase deficiency
- 31 December 1991
- journal article
- Published by Elsevier in Biochemical Medicine and Metabolic Biology
- Vol. 46 (3) , 373-379
- https://doi.org/10.1016/0885-4505(91)90085-y
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation.Journal of Clinical Investigation, 1990
- LIPID STORAGE MYOPATHY ASSOCIATED WITH LOW ACYL-COA DEHYDROGENASE ACTIVITIESBrain, 1988
- Purification and properties of short chain acyl-CoA, medium chain acyl-CoA, and isovaleryl-CoA dehydrogenases from human liver.Published by Elsevier ,1987
- Biosynthesis of Variant Medium Chain Acyl-CoA Dehydrogenase in Cultured Fibroblasts from Patients with Medium Chain Acyl-CoA Dehydrogenase DeficiencyPediatric Research, 1986
- Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblastsBiochemical Medicine, 1985
- Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria. Isolation of the holo- and apoenzymes and conversion of the apoenzyme to the holoenzyme.Journal of Biological Chemistry, 1985