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Another mitochondrial disorder, the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes), is usually caused by mutations in mitochondrial tRNA genes and is associated with impaired assembly and function of complexes I or IV [13, 14]

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The exclusion criteria included the identification of and previous treatment for psychiatric disorders

Loss-of-function of Tet1 in AD mouse models exacerbates A plaque accumulation

Final internal handling, preparation, storage logs, and acceptance procedures should always follow the receiving institutions own SOPs, quality systems, and compliance standards