Funder
National Institute of Neurological Disorders and Stroke
National Institute of Child Health and Human Development
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference45 articles.
1. Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy. Science 242:1427–1430
2. Man PYW, Griffiths PG, Hudson G, Chinnery PF (2009) Inherited mitochondrial optic neuropathies. J Med Genet 46:145–158
3. Carelli V, La Morgia C, Valentino ML, Barboni P, Ross-Cisneros FN, Sadun AA (2009) Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders. BiochimBiophysActa 1787:518–528
4. Brown MD, Torroni A, Reckord LC, Wallace DC (1995) Phylogenetic analysis of Leber’s hereditary optic neuropathy mitochondrial DNA’s indicates multiple independent occurrences of the common mutations. Hum Mutat 6:311–325
5. Carelli V, Ross-Cisneros F, Sadun A (2004) Mitochondrial dysfunction as a cause of optic neuropathies. ProgRetin Eye Res 23:53–89
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