1. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber’s hereditary optic neuropathy
    Jie Shuai et al, 2021, 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. Leber’s Hereditary Optic Neuropathy with visual recovery caused by two rare mutations
    Eli Kisilevsky et al, 2021, Ophthalmic Genetics CrossRef
  5. tRNA variants causing Leber’s hereditary optic neuropathy?
    Josef Finsterer, 2021, Irish Journal of Medical Science (1971 -) CrossRef
  6. 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
  7. Mitochondrial tRNA mutations in Chinese children with tic disorders
    Peifang Jiang et al, 2020, Bioscience Reports CrossRef
  8. Leber’s Hereditary Optic Neuropathy: the roles of mitochondrial transfer RNA variants
    Yu Ding et al, 2021, PeerJ CrossRef
  9. 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
  10. Mechanistic insights into mitochondrial tRNAAla 3’-end metabolism deficiency
    Yanchun Ji et al, 2021, Journal of Biological Chemistry CrossRef