1. A Japanese Case of Leber’s Hereditary Optic Neuropathy with the m.13051G>A Pathogenic Variant
   Yasuyuki Takai et al, 2024, Neuro-Ophthalmology CrossRef
2. tRNA variants causing Leber’s hereditary optic neuropathy?
   Josef Finsterer, 2022, Irish Journal of Medical Science (1971 -) CrossRef
3. Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation
   Agnieszka Piotrowska-Nowak et al, 2020, Metabolic Brain Disease CrossRef
4. Leber’s hereditary optic neuropathy: Update on current diagnosis and treatment
   Ali Esmaeil et al, 2023, Frontiers in Ophthalmology CrossRef
5. Mitochondrial Genetic Heterogeneity in Leber’s Hereditary Optic Neuropathy: Original Study with Meta-Analysis
   Rajan Kumar Jha et al, 2021, Genes CrossRef
6. Genetic Diversity Analysis of the Chinese Daur Ethnic Group in Heilongjiang Province by Complete Mitochondrial Genome Sequencing
   Mansha Jia et al, 2022, Frontiers in Genetics CrossRef
7. Enrichment of retinal ganglion and Müller glia progenitors from retinal organoids derived from human induced pluripotent stem cells - possibilities and current limitations
   Kristine Karla Freude et al, 2020, World Journal of Stem Cells CrossRef