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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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LXR inverse agonists hence improve insulin sensitivity in dysmetabolic rodents

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It should not be used by children under 17 years of age

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Headache , 43 (5), 490495

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The importance of Ca(2+) influx into the neutrophils through TRPV1 channels in the pathogenesis of the patients with PCOS

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10.1016/j.cell.2011.11.050 101 Possemato R., Marks K

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