Mitochondrial encephalomyopathies: Back to mendelian genetics

This publication has 19 references indexed in Scilit:

• Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I
  Annals of Neurology, 1999
• Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
  Annals of Neurology, 1999
• Mitochondrial DNA and Diseases of the Nervous System: The Spectrum
  The Neuroscientist, 1998
• Genetic heterogeneity in leigh syndrome
  Annals of Neurology, 1996
• Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
  Nature Genetics, 1995
• The development of mitochondrial medicine.
  Proceedings of the National Academy of Sciences, 1994
• The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome
  Annals of Neurology, 1993
• Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy
  Science, 1988
• Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
  Nature, 1988
• INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS
  The Journal of cell biology, 1963