Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

Antzeko izenburuak

• MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.
  nork: Chomyn, A, et al.
  Argitaratua: (1992)
• The mutation rate of the human mtDNA deletion mtDNA4977.
  nork: Shenkar, R., et al.
  Argitaratua: (1996)
• RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy
  nork: Reyes, Aurelio, et al.
  Argitaratua: (2015)
• Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
  nork: Koga, Y, et al.
  Argitaratua: (1993)
• Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations
  nork: Chen, Hsiuchen, et al.
  Argitaratua: (2010)