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Description
Comprehensive safety assessment of l-lysine supplementation from clinical studies: A systematic review
Mutations in the major carnitine transporter, encoded by the SLC22A5 gene (also known as zwitterion/cation transporter 2 (OCTN2), are the predominant causes of primary carnitine deficiency (correctly identified as carnitine deficiency, systemic primary)
27 September 2018
The Israel Medical Association journal
