Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation.
Ueda S, Yagi M, Tomoda E, Matsumoto S, Ueyanagi Y, Do Y, Setoyama D, Matsushima Y, Nagao A, Suzuki T, Ide T, Mori Y, Oyama N, Kang D, Uchiumi T.
Ueda S, et al. Among authors: yagi m.
Nucleic Acids Res. 2023 Aug 11;51(14):7480-7495. doi: 10.1093/nar/gkad591.
Nucleic Acids Res. 2023.
PMID: 37439353
Free PMC article.