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The distinct microbiome profile of 5A-1MQ-treated mice was also supported by k-means clustering

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

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With its ability to enter cells directly and present to the cytosol for mitochondrial entry, it may help replenish cellular glutathione levels efficiently, which is essential for maintaining optimal liver function and immune health

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