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[DOI] [PubMed] [Google Scholar] 43.Garca-Lpez D, Cuevas MJ, Almar M, Lima E, De Paz JA, Gonzlez-Gallego J

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

Molecular Events linking oxidative stress and inflammation to insulin resistance and-cell dysfunction

Further investigation is needed to disentangle the roles of biological, environmental, and genetic factors underlying the effects 95,96 and to uncover the mechanisms through which alcohol shapes lipid metabolism and cardiometabolic risk