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Description
Primary and secondary carnitine deficiency syndromes

(More information) L-Carnitine supplementation is indicated for the treatment of primary systemic carnitine deficiency, which is caused by mutations in the gene that codes for the carnitine transporter, OCTN2

Thyroid Hormones : It may interfere with the absorption or effectiveness of thyroid hormones, particularly in people with hypothyroidism

[DOI] [PMC free article] [PubMed] [Google Scholar] 129.Calabrese V, Scapagnini G, Ravagna A, Bella R, Butterfield DA, Calvani M, Pennisi G, Giuffrida Stella AM
