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

مواد مشابهة

• 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.
  بواسطة: Chomyn, A, وآخرون
  منشور في: (1992)
• The mutation rate of the human mtDNA deletion mtDNA4977.
  بواسطة: Shenkar, R., وآخرون
  منشور في: (1996)
• RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy
  بواسطة: Reyes, Aurelio, وآخرون
  منشور في: (2015)
• Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
  بواسطة: Koga, Y, وآخرون
  منشور في: (1993)
• Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations
  بواسطة: Chen, Hsiuchen, وآخرون
  منشور في: (2010)