Mitochondrial diseases: genotype versus phenotype

This publication has 31 references indexed in Scilit:

• Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease
  Mutation Research/DNAging, 1992
• DISEASES OF THE MITOCHONDRIAL DNA
  Annual Review of Biochemistry, 1992
• Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
  Nature Genetics, 1992
• Multiple mitochondrial DNA deletions in an elderly human individual
  FEBS Letters, 1992
• Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease
  Published by American Medical Association (AMA) ,1991
• Age-dependent increase in deleted mitochondrial DNA in the human heart: Possible contributory factor to presbycardia
  American Heart Journal, 1991
• Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation
  Cell, 1990
• Detection of a specific mitochondrial DNA deletion in tissues of older humans
  Nucleic Acids Research, 1990
• Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy
  Science, 1988
• Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
  Nature, 1988