Inheritance of mitochondrial disorders

This publication has 47 references indexed in Scilit:

• Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication
  Human Molecular Genetics, 2001
• Epidemiology and treatment of mitochondrial disorders
  American Journal of Medical Genetics, 2001
• Random Genetic Drift Determines the Level of Mutant mtDNA in Human Primary Oocytes
  American Journal of Human Genetics, 2001
• Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?
  American Journal of Medical Genetics, 2001
• The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
  Trends in Genetics, 2000
• Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene
  Annals of Neurology, 2000
• The epidemiology of pathogenic mitochondrial DNA mutations
  Annals of Neurology, 2000
• MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring
  Brain, 1998
• Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
  Brain, 1997
• Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
  Nature Genetics, 1995