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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

People with malabsorption are more likely to have B12 deficiency

Tips for Optimal Use Follow Your Doctors Instructions: Always follow the dosing schedule and instructions provided by your healthcare provider

UK nutrition legislation guidance Food Standards Agency

The difference between winning and losing can often come down to small differences in muscle recovery and endurance time