Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

Những quyển sách tương tự

• De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome.
  Bằng: Takahashi, S, et al.
  Được phát hành: (1998)
• Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.
  Bằng: Tatuch, Y, et al.
  Được phát hành: (1992)
• Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes.
  Bằng: Blok, R B, et al.
  Được phát hành: (1997)
• Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells
  Bằng: Trounce, Ian, et al.
  Được phát hành: (2000)
• The frequency of mtDNA 8994 polymorphism and detection of the NARP 8993 mutation
  Bằng: Gray, R, et al.
  Được phát hành: (2002)