논문KCI 등재
Clinical Features of Leber Hereditary Optic Neuropathy Carrying a Rare m.13051G>A Mitochondrial Mutation: A Case Report
대한안과학회 (The Korean Ophthalmological Society)|2025.12|Korean Journal of Ophthalmology|제39권 제6호|pp. 586-588
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Leber Hereditary Optic Neuropathy and Stroke-Like Lesions Associated With MT-ND5 m.13513G>A Mutation: A Case Report김성태, 김용식, 임채영대한자기공명의과학회 · Investigative Magnetic Resonance Imaging2025 · 제29권 제2호Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA DeletionsJosef Finsterer연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제2호Mitochondrial Retinopathy by MT-ATP6 Variant Revealed by Whole-Genome Sequencing: A Case ReportJaehwan Choi, Ja-Hyun Jang, Sang Jin Kim, Sungsoon Hwang대한안과학회 · Korean Journal of Ophthalmology2024 · 제38권 제4호Leber’s ‘Plus’ in a Korean Patient with 14484/ND6 Mutation김승희, 김지수대한신경과학회 · Journal of Clinical Neurology2016 · 제12권 제4호Leber’s Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNAEmi Fusayasu, Kazuhiro Nakaso, Keiko Imamura, Kenichi Yasui, Kenji Nakashima, Koji Doi, Yoshiki Adachi대한신경과학회 · Journal of Clinical Neurology2012 · 제8권 제3호The Author Reply: Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions이영목연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제2호
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