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

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ADSCs-derived exosomes ameliorate hepatic fibrosis by suppressing stellate cell activation and remodeling hepatocellular glutamine synthetase-mediated glutamine and ammonia homeostasis

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It is also sensible to speak with a doctor before starting l carnitine in the setting of chronic kidney disease, dialysis, pregnancy, breastfeeding, or multiple medications

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