The role of APOE in the phenotypic expression of Leber hereditary optic neuropathy

J Med Genet. 2003 Apr;40(4):e41. doi: 10.1136/jmg.40.4.e41.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Apolipoproteins E / genetics*
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism
  • DNA Mutational Analysis
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • England
  • Family Health
  • Female
  • Genotype
  • Humans
  • Italy
  • Logistic Models
  • Male
  • Optic Atrophy, Hereditary, Leber / genetics*
  • Optic Atrophy, Hereditary, Leber / pathology
  • Phenotype
  • Point Mutation
  • Survival Analysis

Substances

  • Apolipoproteins E
  • DNA
  • Deoxyribonucleases, Type II Site-Specific
  • GCGC-specific type II deoxyribonucleases

Associated data

  • OMIM/535000