mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?

This publication has 19 references indexed in Scilit:

• Leber Hereditary Optic Neuropathy: How Do Mitochondrial DNA Mutations Cause Degeneration of the Optic Nerve?
  Journal of Bioenergetics and Biomembranes, 1997
• Dominant Optic Atrophy, Kjer Type
  Archives of Ophthalmology (1950), 1997
• Clinical and Genetic Analysis of a Family Affected With Dominant Optic Atrophy (OPA1)
  Archives of Ophthalmology (1950), 1997
• Increased risk of dementia in mothers of Alzheimer's disease cases
  Neurology, 1996
• Ophthalmologic Findings in Leber Hereditary Optic Neuropathy, with Special Reference to mtDNA Mutations
  Ophthalmology, 1996
• MITOMAP: a human mitochondrial genome database
  Nucleic Acids Research, 1996
• A mitochondrial DNA clone is associated with increased risk for Alzheimer disease.
  Proceedings of the National Academy of Sciences, 1995
• Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations
  Human Mutation, 1995
• A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
  Proceedings of the National Academy of Sciences, 1994
• Sequence and organization of the human mitochondrial genome
  Nature, 1981