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Mitochondrion|September 8, 2014
Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese familiesJuanjuan Zhang, Pingping Jiang, Xiaofen Jin, et al.Journal of Human Genetics|January 17, 2014
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese familiesYanchun Ji, Min Liang, Juanjuan Zhang, et al.Investigative Ophthalmology & Visual Science|July 29, 2015
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic NeuropathyPingping Jiang, Min Liang, Juanjuan Zhang, et al.Ophthalmology|December 7, 2010
Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese familiesXiao-Ling Liu, Xiangtian Zhou, Jian Zhou, et al.Investigative Ophthalmology & Visual Science|January 9, 2014
Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathyMin Liang, Pingping Jiang, Feng Li, et al.The Journal of Clinical Investigation|June 10, 2020
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathyJialing Yu, Xiaoyang Liang, Yanchun Ji, et al.Human Molecular Genetics|December 10, 2015
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 mutationPingping Jiang, Xiaofen Jin, Yanyan Peng, et al.Human Molecular Genetics|January 1, 2019
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathyYanchun Ji, Juanjuan Zhang, Jialing Yu, et al.Pageof 5