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Description
Primary carnitine deficiency PCD is a rare genetic disease caused by mutations in the SLC22A5 gene, which leads to dysfunction of the carnitine transporter OCTN2, thereby hindering the entry of carnitine from the blood into cells and the reabsorption of carnitine by the kidneys

The club's annual membership drive added ninety-two members

Ascorbylated 4-hydroxy-2-nonenal as a potential biomarker of oxidative stress response
Results The effect of dietary L-carnitine supplementation on the carnitine concentration, carnitine synthesis gene expression and triglyceride levels in tissues During the experiment, the fish were in good health and showed no growth differences compared with control fish (data not shown)

Mean platelet volume and coronary plaque vulnerability: an optical coherence tomography study in patients with non-ST-elevation acute coronary syndrome

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