Min Liang

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

Pingping Jiang, Xiaofen Jin, Yanyan Peng et al. · Human Molecular Genetics · 2015 · 103 citations · Full text

Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

Min Liang, Minqiang Guan, Fuxin Zhao et al. · Biochemical and Biophysical Research Communications · 2009 · 78 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +13

Prevalence of Mitochondrial<i>ND4</i>Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy

Pingping Jiang, Min Liang, Juanjuan Zhang et al. · Investigative Ophthalmology & Visual Science · 2015 · 59 citations

Mitochondrial<i>ND1</i>Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy

Yanchun Ji, Min Liang, Juanjuan Zhang et al. · Investigative Ophthalmology & Visual Science · 2016 · 48 citations · Full text

Frequency and Spectrum of Mitochondrial<i>ND6</i>Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy

Min Liang, Pingping Jiang, Feng Li et al. · Investigative Ophthalmology & Visual Science · 2014 · 46 citations