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- ...t T, Suomalainen A (2018) Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor |authors=Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, Loennqvist T, Suomalainen Anu2 KB (212 words) - 09:20, 18 March 2020