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There are a bunch of other inborn errors of metabolism, including short-chain acyl-CoA dehydrogenase deficiency and medium-chain acyl-CoA dehydrogenase deficiency.[ref] Lets look at the inborn errors of metabolism involving carnitine: CPT2 gene: The CPT2 gene encodes the enzyme that moves fatty acids attached to carnitine into the inner membrane of the mitochondria
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The 200% GLP-1 increase claim, while possibly accurate in percentage terms, obscures the fundamental limitation that natural GLP-1 degrades in minutes while pharmaceutical alternatives act for days
Int J Mol Sci 23:10864
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