mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?
- 1 January 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (1), 196-202
- https://doi.org/10.1086/301675
Abstract
No abstract availableKeywords
This publication has 16 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 TypeArchives 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 casesNeurology, 1996
- Ophthalmologic Findings in Leber Hereditary Optic Neuropathy, with Special Reference to mtDNA MutationsOphthalmology, 1996
- MITOMAP: a human mitochondrial genome databaseNucleic 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 mutationsHuman 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 genomeNature, 1981