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Mechanistic insights into mitochondrial tRNAAla 3'-end metabolism deficiency.
Ji Y, Nie Z, Meng F, Hu C, Chen H, Jin L, Chen M, Zhang M, Zhang J, Liang M, Wang M, Guan MX. Ji Y, et al. Among authors: zhang m, zhang j. J Biol Chem. 2021 Jul;297(1):100816. doi: 10.1016/j.jbc.2021.100816. Epub 2021 May 21. J Biol Chem. 2021. PMID: 34023389 Free PMC article.
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.
Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Zhang Z, Ji Y, Zhang J, Liang M, Zhao F, Sun YH, Zhang M, Zhou X, Chen Y, Mo JQ, Huang T, Qu J, Guan MX. Jiang P, et al. Among authors: zhang m, zhang z, zhang j. Hum Mol Genet. 2016 Feb 1;25(3):584-96. doi: 10.1093/hmg/ddv498. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647310
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