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mt atp6 protein, human
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Probing the pathogenicity of patient-derived variants of MT-ATP6 in yeast.
Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with…
MT-ATP6 mitochondrial disease identified by newborn screening reveals a distinct biochemical phenoty…
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.
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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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