Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency

J Inherit Metab Dis. 1995;18(2):173-6. doi: 10.1007/BF00711759.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Brain Diseases, Metabolic / diagnosis*
  • Child
  • Child, Preschool
  • Disease Progression
  • Glutaryl-CoA Dehydrogenase
  • Humans
  • Infant
  • Oxidoreductases / deficiency*
  • Oxidoreductases Acting on CH-CH Group Donors*

Substances

  • Oxidoreductases
  • Oxidoreductases Acting on CH-CH Group Donors
  • Glutaryl-CoA Dehydrogenase