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Brain, ISSN 0006-8950, 2009, Volume 132, Issue 9, pp. 2317 - 2326
Leber hereditary optic neuropathy (LHON) is a genetic disorder primarily due to mutations of mitochondrial DNA (mtDNA). Environmental factors are thought to... 
Epigenetics | Alcohol | Leber hereditary optic neuropathy | Tobacco | Mitochondrial DNA | alcohol | MITOCHONDRIAL-DNA MUTATIONS | DISCORDANT | mitochondrial DNA | CLINICAL EXPRESSION | SMOKING | LOCUS | NEUROSCIENCES | epigenetics | CLINICAL NEUROLOGY | PEDIGREES | DISEASE | tobacco | IDENTICAL-TWINS | EXPOSURE
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2012, Volume 109, Issue 49, pp. 20065 - 20070
An animal model of Leber hereditary optic neuropathy (LHON) was produced by introducing the human optic atrophy mtDNA ND6 P25L mutation into the mouse. Mice... 
Axons | Mitochondria | Optic atrophy | Optic nerve | Leber hereditary optic atrophy | Cell lines | Mitochondrial DNA | Biochemistry | Synaptosomes | Genetic mutation | Neurodegenerative disease | Ophthalmology | Oxidative phosphorylation | Maternal inheritance | LIFE-SPAN | neurodegenerative disease | MULTIDISCIPLINARY SCIENCES | MITOCHONDRIAL-DNA MUTATION | CELL LINES | maternal inheritance | oxidative phosphorylation | GLUTAMATE TRANSPORT | ENCEPHALOPATHY | RESPIRATORY COMPLEX I | ophthalmology | MICE | CYBRIDS | DYSFUNCTION | SUPEROXIDE-DISMUTASE | Electroretinography | Optic Nerve - pathology | Optic Atrophy, Hereditary, Leber - complications | Reactive Oxygen Species - metabolism | Age Factors | Humans | Oxidative Stress - physiology | Immunoblotting | NADH Dehydrogenase - genetics | Optic Atrophy, Hereditary, Leber - genetics | Synaptosomes - metabolism | Mutation, Missense - genetics | Animals | DNA, Mitochondrial - genetics | Adenosine Triphosphate - metabolism | Demyelinating Diseases - etiology | Mice | Demyelinating Diseases - pathology | Optic Atrophy, Hereditary, Leber - physiopathology | Retina - pathology | Disease Models, Animal | Development and progression | Genetic aspects | Gene mutations | Health aspects | Oxidative stress | Rodents | Retina | Mutation | Adenosine triphosphatase | Index Medicus | Biological Sciences
Journal Article
Brain, ISSN 0006-8950, 01/2011, Volume 134, Issue 1, pp. 220 - 234
Journal Article
Journal Article
Brain, ISSN 0006-8950, 2014, Volume 137, Issue 2, pp. 335 - 353
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 02/2019, Volume 97, Issue 1, pp. e71 - e76
Journal Article
Vestnik Oftalmologii, ISSN 0042-465X, 2018, Volume 134, Issue 2, pp. 92 - 96
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 06/2018, Volume 235, Issue 6, pp. 747 - 763
Journal Article
Journal Article
Neuro-Ophthalmology Japan, ISSN 0289-7024, 2017, Volume 34, Issue 2, pp. 190 - 195
Journal Article
Neurology, ISSN 0028-3878, 11/2016, Volume 87, Issue 19, pp. 2065 - 2066
A 17-year-old man had acute vision loss OS (visual acuity 20/40), having lost vision OD months before (20/400). There were cecocentral scotomas OU.... 
CLINICAL NEUROLOGY | Optic Atrophy, Hereditary, Leber - diagnostic imaging | Male | Tomography, Optical Coherence - methods | Angiography - methods | Humans | Adolescent | Index Medicus | Abridged Index Medicus
Journal Article
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