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The reported patient A had two homozygous variants: one pathogenic CPT II gene, confirming CPT II deficiency and a likely pathogenic variant in SLC22A5 gene indicating primary carnitine deficiency (Table 1)

doi: 10.1038/ni.2956 15 KoelwynGJCorrEMErbayEMooreKJ

Australian Journal of Experimental Agriculture 48: 1341-1344.Google Scholar HARPAZ, S., BECKER, K

& Pietrzykowski, P

Pyruvate-supported flux through medium-chain ketothiolase promotes mitochondrial lipid tolerance in cardiac and skeletal muscles

NAM and streptozotocin (STZ)-induced T2DM also leads to hepatic damage, including disrupted antioxidant status, aberrant intrahepatic lipid accumulation, and inflammation
