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[DOI] [PubMed] [Google Scholar] Acosta M.F., Muralidhran P., Abrahamson M.D., Grijalva C.L., Carver M., Tang H., Klinger C., Fineman J.R., Black S.M., Mansour H.M

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Defects in the carnitine transporter (OCTN2), which is coded by the SLC22A5 gene, create primary carnitine deficiency, expressed as low urinary carnitine excretion and low blood and tissues carnitine level, which may be a risk factor of ASD

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