Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

J Inherit Metab Dis. 1990;13(3):311-4. doi: 10.1007/BF01799383.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Cells, Cultured
  • Fatty Acids / metabolism*
  • Female
  • Fibroblasts / enzymology
  • Humans
  • Infant
  • Mitochondria / enzymology*
  • Oxidation-Reduction

Substances

  • Fatty Acids
  • 3-Hydroxyacyl CoA Dehydrogenases