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.

MLA

Jiang, Pingping, et al. “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.” Human Molecular Genetics, vol. 25, no. 3, Feb. 2016, pp. 584–96. EBSCOhost, https://doi.org/10.1093/hmg/ddv498.

APA

Jiang, P., Jin, X., Peng, Y., Wang, M., Liu, H., Liu, X., Zhang, Z., Ji, Y., Zhang, J., Liang, M., Zhao, F., Sun, Y.-H., Zhang, M., Zhou, X., Chen, Y., Mo, J. Q., Huang, T., Qu, J., & Guan, M.-X. (2016). 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. Human Molecular Genetics, 25(3), 584–596. https://doi.org/10.1093/hmg/ddv498

Chicago

Jiang, Pingping, Xiaofen Jin, Yanyan Peng, Meng Wang, Hao Liu, Xiaoling Liu, Zengjun Zhang, et al. 2016. “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.” Human Molecular Genetics 25 (3): 584–96. doi:10.1093/hmg/ddv498.