Reassessment of the pathologic significance of the 9438 mitochondrial DNA mutation associated with LHON

Ophthalmic Genet. 2007 Dec;28(4):229-30. doi: 10.1080/13816810701639741.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • DNA, Mitochondrial / genetics*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Optic Atrophy, Hereditary, Leber / genetics*

Substances

  • DNA, Mitochondrial