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• W2238145246 endingPage "117" @default.
• W2238145246 startingPage "109" @default.
• W2238145246 abstract "Mitochondrial diseases are clinically and genetically heterogeneous disorders, which make their exact diagnosis and classification difficult. The purpose of this study was to identify pathogenic mitochondrial DNA (mtDNA) mutations in 2 Korean families with myoclonic epilepsy with ragged-red fibers (MERRF) and Leigh syndrome, respectively." @default.
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• W2238145246 date "2015-12-31" @default.
• W2238145246 modified "2023-10-02" @default.
• W2238145246 title "Identification of causative mutations in patients with Leigh syndrome and MERRF by mitochondrial DNA-targeted next-generation sequencing" @default.
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• W2238145246 doi "https://doi.org/10.5734/jgm.2015.12.2.109" @default.
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