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(Zhejiang University), Min‐Xin Guan(Zhejiang University), Zengjun Zhang(Wenzhou Medical University), Taosheng Huang(The Centre for Health (New Zealand)), Min Liang(Zhejiang Institute of Mechanical and Electrical Engineering), Fuxin Zhao(Wenzhou Medical University), Yanyan Peng(First Hospital of Shijiazhuang), Yanchun Ji(Children's Hospital of Zhejiang University), Ye Chen(Anhui Medical University), Meng Wang(Chinese Academy of Sciences), Xiaoling Liu(Wenzhou Medical University), Juanjuan Zhang(Wenzhou Medical University), Hao Liu(Gansu Coalfield Geology Bureau), Xiaofen Jin(Zhejiang Institute of Mechanical and Electrical Engineering), Yanhong Sun(Yunnan Center for Disease Control And Prevention), Jun Qin Mo(Rady Children's Hospital-San Diego), Xiangtian Zhou(Wenzhou Medical University), Jia Qu(Wenzhou Medical University), Minglian Zhang(Hebei Medical University)
Human Molecular Genetics
December 8, 2015
Cited by 103


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