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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H., Bergmann, M
These individuals may lose 10 lbs or more in the first month even on the lowest dose due to high genetic sensitivity to the medication. Months 23: The Steady Climb As you move up to the second and third dose strengths, the metabolic changes become more profound
