Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.

Eitemau Tebyg

• Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
  gan: Mita, S, et al.
  Cyhoeddwyd: (1989)
• Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
  gan: Nelson, I, et al.
  Cyhoeddwyd: (1989)
• Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.
  gan: Mita, S, et al.
  Cyhoeddwyd: (1990)
• Loss of Myelin-Associated Glycoprotein in Kearns-Sayre Syndrome
  gan: Lax, Nichola Z., et al.
  Cyhoeddwyd: (2012)
• MERRF and Kearns-Sayre overlap syndrome due to the mtDNA m.3291T>C mutation
  gan: Emmanuele, Valentina, et al.
  Cyhoeddwyd: (2011)