doi: 10.1007/s11154-019-09512-0 79 GurungMLiZYouHRodriguesRJumpDBMorgunAet al
Primary carnitine deficiency (carnitine deficiency, systemic primary: CDSP) is an autosomal recessive disorder that results from the lack of function of the carnitine transporter, OCTN2
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This occurs via the carnitine palmitoyltransferase (CPT) system, with CPT1 aiding the transport of fatty acids into the mitochondria and CPT2 facilitating their release once processed
Studies suggest that including a source of protein at each meal may help increase postprandial GLP-1 levels