Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders

Mol Genet Metab. Sep-Oct 2000;71(1-2):93-9. doi: 10.1006/mgme.2000.3014.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • DNA, Mitochondrial / genetics*
  • Humans
  • Mitochondrial Myopathies / etiology
  • Mitochondrial Myopathies / genetics*
  • Mutation
  • Organ Specificity
  • Phenotype
  • Presbycusis / etiology
  • Presbycusis / genetics

Substances

  • DNA, Mitochondrial