1. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber’s hereditary optic neuropathy
   Jie Shuai et al, 2022, Irish Journal of Medical Science (1971 -) CrossRef
2. The mitochondrial tRNAAla 5587T>C and tRNALeu(CUN) 12280A>G mutations may be associated with hypertension in a Chinese family
   Lin Lin et al, 2018, Experimental and Therapeutic Medicine CrossRef
3. Maternally Inherited Diabetes Mellitus Associated with a Novel m.15897G>A Mutation in Mitochondrial tRNAThr Gene
   Ke Li et al, 2020, Journal of Diabetes Research CrossRef
4. tRNA variants causing Leber’s hereditary optic neuropathy?
   Josef Finsterer, 2022, Irish Journal of Medical Science (1971 -) CrossRef
5. Novel mitochondrial tRNALeu(UUR) 3261A > g mutation in two pedigrees with essential hypertension
   Ye Fu et al, 2023, Irish Journal of Medical Science (1971 -) CrossRef
6. Mitochondrial tRNA mutations in Chinese children with tic disorders
   Peifang Jiang et al, 2020, Bioscience Reports CrossRef
7. Leber’s Hereditary Optic Neuropathy: the roles of mitochondrial transfer RNA variants
   Yu Ding et al, 2021, PeerJ CrossRef
8. Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber’s hereditary optic neuropathy
   Ye Jin Ahn et al, 2020, Graefe's Archive for Clinical and Experimental Ophthalmology CrossRef
9. Mechanistic insights into mitochondrial tRNAAla 3’-end metabolism deficiency
   Yanchun Ji et al, 2021, Journal of Biological Chemistry CrossRef
10. Maternally transmitted diabetes mellitus may be associated with mitochondrial ND5 T12338C and tRNAAla T5587C variants
    Zhaochang Jiang et al, 2022, Irish Journal of Medical Science (1971 -) CrossRef
11. Leber’s Hereditary Optic Neuropathy with visual recovery caused by two rare mutations
    Eli Kisilevsky et al, 2021, Ophthalmic Genetics CrossRef
12. Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus
    Liangyan Lin et al, 2021, International Journal of General Medicine CrossRef
13. Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families
    Li-Jing Zhao et al, 2022, World Journal of Clinical Cases CrossRef