Jul 2026
Mitochondrial tRNAGly A10055G mutation contributes to non-syndromic hearing loss: a study of three Han Chinese pedigrees
Findings indicated that the m.A10055G mutation contributed to NSHL pathogenesis by impairing mitochondrial functions, most likely through defective tRNA metabolism and by increasing oxidative stress.
Xiao-Xiang Chen, Xiu-Mei He, Yun Li et al.
· Mitochondrial DNA. Part A, D... · 0 citations