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As more real-world data continues to pour in, researchers are now meticulously studying side effects and potential complications

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

(se han cocido los huesos con verdura, carne y garbanzos) Mil gracias

Fatty acid import into mitochondria