Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement

J Med Genet. 1999 Dec;36(12):934-5.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Causality
  • Cell Nucleus / genetics
  • DNA, Mitochondrial / genetics*
  • Gene Deletion*
  • Humans
  • MELAS Syndrome / genetics
  • Mitochondrial Myopathies / genetics*
  • Optic Atrophies, Hereditary / genetics

Substances

  • DNA, Mitochondrial