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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
Clinical Ophthalmology, ISSN 1177-5467, 06/2015, Volume 9, pp. 1165 - 1176
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
Journal Article
Current opinion in neurology, ISSN 1350-7540, 02/2019, Volume 32, Issue 1, pp. 99 - 104
Purpose of review Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial DNA (mtDNA) disorder in the population and it carries a... 
STEM-CELLS | LIGHT | gene therapy | NEUROSCIENCES | mitochondrial disease | CLINICAL NEUROLOGY | RETINAL GANGLION-CELLS | COPY NUMBER | Leber hereditary optic neuropathy | retinal ganglion cells | GENE-THERAPY | GENERATION | FUNCTIONAL AXONS | idebenone | Usage | Research | Gene mutations | Gene therapy
Journal Article
Brain, ISSN 0006-8950, 01/2011, Volume 134, Issue 1, pp. 220 - 234
Journal Article
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 02/2019, Volume 97, Issue 1, pp. e71 - e76
Journal Article
Brain, ISSN 0006-8950, 2014, Volume 137, Issue 2, pp. 335 - 353
Journal Article
ISSN 1350-7540, 2019
Journal Article
Vestnik oftalmologii, ISSN 0042-465X, 2018, Volume 134, Issue 2, p. 92
Leber hereditary optic neuropathy is characterized by bilateral, painless loss of vision in children and young adults (generally up to 25 years old). Since its... 
Young Adult | Humans | Adult | DNA, Mitochondrial | Mutation | Ophthalmology | Optic Atrophy, Hereditary, Leber - diagnosis | Child
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
by Wan, X and Pei, H and Zhao, MJ and Yang, S and Hu, WK and He, H and Ma, SQ and Zhang, G and Dong, XY and Chen, C and Wang, DW and Li, B
SCIENTIFIC REPORTS, ISSN 2045-2322, 02/2016, Volume 6, p. 21587
Leber's hereditary optic neuropathy (LHON) is a mitochondrially inherited disease leading to blindness. A mitochondrial DNA point mutation at the 11778... 
COMPLEX-I | MULTIDISCIPLINARY SCIENCES | IDEBENONE | DISEASE | LHON | MITOCHONDRIAL DYSFUNCTION | GENE-THERAPY | MUTATIONS |