Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes

This publication has 41 references indexed in Scilit:

• Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA
  Nature Genetics, 1996
• Leigh syndrome: Clinical features and biochemical and DNA abnormalities
  Annals of Neurology, 1996
• The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome
  Annals of Neurology, 1993
• Noninvasive diagnosis of the MELAS syndrome from blood DNA
  Annals of Neurology, 1993
• Quantification of tRNA₃₂₄₃^Leu point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription
  Human Molecular Genetics, 1993
• Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy
  Biochemical and Biophysical Research Communications, 1990
• Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
  Annals of Neurology, 1989
• DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING
  Published by Elsevier ,1989
• Sequence and organization of the human mitochondrial genome
  Nature, 1981
• ROLE OF THE MITOCHONDRIAL GENOME DURING EARLY DEVELOPMENT IN MICE
  The Journal of cell biology, 1973