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Methylcobalamin acts as a cofactor for the enzyme methionine synthase, which is essential for converting homocysteine to methionine and supporting methylation processes throughout the body

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1988 Jun;24(2):162-72

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Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: Implications for pathogenesis and treatment