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Model for the transmembrane helices of the ATP6 subunit of the F 1 F... | Download Scientific Diagram
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A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism | SpringerLink
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MT‐ATP6 mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases - Ganetzky - 2019 - Human Mutation - Wiley Online Library
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Association of a point mutation (m.9176T>G) of the MT-ATP6 gene with Leigh syndrome: A case report | Biomedical Research and Therapy
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Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human cancer, affect ROS, calcium homeostasis and mitochondrial permeability transition in yeast - ScienceDirect
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IJMS | Free Full-Text | A Mutation in Mouse MT-ATP6 Gene Induces Respiration Defects and Opposed Effects on the Cell Tumorigenic Phenotype
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PDF] Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human cancer, affect ROS, calcium homeostasis and mitochondrial permeability transition in yeast. | Semantic Scholar
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Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis | bioRxiv
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A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome - ScienceDirect
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