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Finally, the enhanced lipid droplet formation in CD37-negative DLBCL tissues of patients supports the translational value of our present findings

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder of fatty acid oxidation caused by deficiency of plasma membrane carnitine transport resulting from impairment in the plasma membrane OCTN2 carnitine transporter

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It facilitates the transportation of fatty acids into the mitochondria, where they are converted into usable energy