Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

Lignende værker

• Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
  af: Nakase, H, et al.
  Udgivet: (1990)
• Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
  af: Mita, S, et al.
  Udgivet: (1989)
• Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region.
  af: Moraes, C T, et al.
  Udgivet: (1991)
• mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.
  af: Moraes, C T, et al.
  Udgivet: (1991)
• The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
  af: Moraes, C T, et al.
  Udgivet: (1992)