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3. Mitochondrial transport mediates survival of retinal ganglion cells in affected LHON patients. Yang TC; Yarmishyn AA; Yang YP; Lu PC; Chou SJ; Wang ML; Lin TC; Hwang DK; Chou YB; Chen SJ; Yu WK; Wang AG; Hsu CC; Chiou SH Hum Mol Genet; 2020 Jun; 29(9):1454-1464. PubMed ID: 32277753 [TBL] [Abstract][Full Text] [Related]
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8. Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy. Asanad S; Tian JJ; Frousiakis S; Jiang JP; Kogachi K; Felix CM; Fatemeh D; Irvine AG; Ter-Zakarian A; Falavarjani KG; Barboni P; Karanjia R; Sadun AA Curr Eye Res; 2019 Jun; 44(6):638-644. PubMed ID: 30649972 [No Abstract] [Full Text] [Related]
9. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. Jiang P; Jin X; Peng Y; Wang M; Liu H; Liu X; Zhang Z; Ji Y; Zhang J; Liang M; Zhao F; Sun YH; Zhang M; Zhou X; Chen Y; Mo JQ; Huang T; Qu J; Guan MX Hum Mol Genet; 2016 Feb; 25(3):584-96. PubMed ID: 26647310 [TBL] [Abstract][Full Text] [Related]
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14. Idebenone protects against retinal damage and loss of vision in a mouse model of Leber's hereditary optic neuropathy. Heitz FD; Erb M; Anklin C; Robay D; Pernet V; Gueven N PLoS One; 2012; 7(9):e45182. PubMed ID: 23028832 [TBL] [Abstract][Full Text] [Related]
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16. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy. Liang M; Jiang P; Li F; Zhang J; Ji Y; He Y; Xu M; Zhu J; Meng X; Zhao F; Tong Y; Liu X; Sun Y; Zhou X; Mo JQ; Qu J; Guan MX Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1321-31. PubMed ID: 24398099 [TBL] [Abstract][Full Text] [Related]
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