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Human Molecular Genetics|July 19, 2016
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutationPingping Jiang, Min Liang, Chaofan Zhang, et al.
The Journal of Biological Chemistry|November 6, 2019
Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutationWenlu Fan, Jing Zheng, Wanzhong Kong, et al.
JCI Insight|December 3, 2020
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing lossLimei Cui, Jing Zheng, Qiong Zhao, et al.
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