Disorders of pyruvate metabolism and the tricarboxylic acid cycle

Mol Genet Metab. 2005 Aug;85(4):243-6. doi: 10.1016/j.ymgme.2005.06.006.
No abstract available

Publication types

  • Review

MeSH terms

  • Brain Diseases, Metabolic, Inborn / genetics
  • Brain Diseases, Metabolic, Inborn / metabolism*
  • Brain Diseases, Metabolic, Inborn / therapy
  • Citric Acid Cycle
  • Fumarate Hydratase / deficiency
  • Fumarate Hydratase / metabolism
  • Humans
  • Ketoglutarate Dehydrogenase Complex / deficiency
  • Ketoglutarate Dehydrogenase Complex / metabolism
  • Pyruvate Carboxylase / metabolism*
  • Pyruvate Carboxylase Deficiency Disease / metabolism
  • Pyruvate Dehydrogenase Complex Deficiency Disease / genetics
  • Pyruvate Dehydrogenase Complex Deficiency Disease / metabolism
  • Succinate Dehydrogenase / deficiency
  • Succinate Dehydrogenase / genetics
  • Succinate Dehydrogenase / metabolism

Substances

  • Ketoglutarate Dehydrogenase Complex
  • Succinate Dehydrogenase
  • Fumarate Hydratase
  • Pyruvate Carboxylase