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Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)

A flood of criminal activity The tremendous demand for GLP-1s has generated so much crime and patient danger that it makes my head spin

38 FBP, fasting blood glucose

Genetic insights into your metabolic profile can help your prescriber anticipate absorption challenges and select antibiotics with the best pharmacokinetic compatibility for your unique biology