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mt atp6 protein, human
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There were no matches for mt atp6 protein, human
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Reply to the letter: "Is the variant m.9176T>C in MT-ATP6 truly responsibly for Leigh syndrome?
Cerebellar Bottom of Fissure Hyperintensities in MT-ATP6-Associated Ataxia.
Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations …
Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome.
Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype-Different Onset.
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Efficacy of a Nutritional Education Strategy and Physical Exercise on the Gut Microbiota in Type 2 D…
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