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A.ArenillasJ.RibM.et al
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
2026;Epub ahead of print
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Severe malarial anemia: innate immunity and pathogenesis
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