Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

This publication has 13 references indexed in Scilit:

• Leber's hereditary optic neuropathy and complex I deficiency in muscle
  Annals of Neurology, 1991
• Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations
  The Journal of Pediatrics, 1991
• Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies
  Annals of Neurology, 1990
• Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease
  Cell, 1990
• Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndrome
  Neurology, 1990
• Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
  Annals of Neurology, 1989
• Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
  New England Journal of Medicine, 1989
• Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies
  Journal of the Neurological Sciences, 1988
• Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?
  Annals of Neurology, 1977
• NONDROPLET ULTRASTRUCTURAL DEMONSTRATION OF CYTOCHROME OXIDASE ACTIVITY WITH A POLYMERIZING OSMIOPHILIC REAGENT, DIAMINOBENZIDINE (DAB)
  The Journal of cell biology, 1968