Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy

Epilepsia. 1999;40 Suppl 3:33-40. doi: 10.1111/j.1528-1157.1999.tb00897.x.
No abstract available

Publication types

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

MeSH terms

  • Calcium / metabolism
  • Calcium / physiology
  • DNA, Mitochondrial / chemistry
  • DNA, Mitochondrial / genetics*
  • DNA, Mitochondrial / physiology
  • Epilepsy / genetics*
  • Epilepsy / metabolism
  • Epilepsy / physiopathology
  • Free Radicals
  • Humans
  • MELAS Syndrome / genetics
  • MELAS Syndrome / metabolism
  • MELAS Syndrome / physiopathology
  • MERRF Syndrome / genetics
  • MERRF Syndrome / metabolism
  • MERRF Syndrome / physiopathology
  • Mitochondrial Encephalomyopathies / genetics*
  • Mitochondrial Encephalomyopathies / metabolism
  • Mitochondrial Encephalomyopathies / physiopathology
  • Mitochondrial Myopathies / genetics*
  • Mitochondrial Myopathies / metabolism
  • Mitochondrial Myopathies / physiopathology
  • Mutation / genetics
  • Neurotoxins / metabolism

Substances

  • DNA, Mitochondrial
  • Free Radicals
  • Neurotoxins
  • Calcium