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<i>DNAJC30</i> defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndromeSarah L. Stenton, Holger Prokisch, Markéta Tesařová et al.|Brain|2022Cited by 46
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Clinical and molecular characteristics of newly reported mitochondrial disease entity caused by biallelic PARS2 mutationsElżbieta Ciara, Ewa Pronicka, Dariusz Rokicki et al.|Journal of Human Genetics|2018Cited by 26
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