3-Methylglutaconic aciduria: a common biochemical marker in various syndromes with diverse clinical features

Mol Genet Metab. 2005 Jan;84(1):1-3. doi: 10.1016/j.ymgme.2004.12.003.
No abstract available

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / metabolism*
  • Acetyl Coenzyme A / metabolism
  • Amino Acid Metabolism, Inborn Errors / metabolism*
  • Glutarates / metabolism*
  • Humans
  • Hydro-Lyases / deficiency*
  • Hydro-Lyases / urine
  • Leucine / metabolism
  • Mitochondrial Diseases / metabolism*
  • Sterols / biosynthesis

Substances

  • Glutarates
  • Sterols
  • 3-methylglutaconic acid
  • Acetyl Coenzyme A
  • Hydro-Lyases
  • methylglutaconyl-CoA hydratase
  • Leucine