Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase

Prog Clin Biol Res. 1992:375:327-37.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Acetyl-CoA C-Acyltransferase / deficiency*
  • Cells, Cultured
  • Enoyl-CoA Hydratase / deficiency*
  • Female
  • Fibroblasts / enzymology
  • Humans
  • Infant
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Metabolism, Inborn Errors / enzymology*
  • Mitochondria, Muscle / enzymology*
  • Oxidation-Reduction

Substances

  • 3-Hydroxyacyl CoA Dehydrogenases
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Acetyl-CoA C-Acyltransferase
  • Enoyl-CoA Hydratase