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Selected publications: Mechanisms of assembly and remodelling of the extracellular matrix Nat Rev Mol Cell Biol , 2024

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)

Consult with a physician: Always consult a healthcare provider before starting any new supplement, especially if you have a pre-existing condition

The National Kidney Foundation recommends treatment of dialysis-related carnitine disorder symptoms with intravenous L-carnitine at 20 mg/kg of total body weight after each dialysis procedure

DOI: 10.1016/j.tem.2017.02.004