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Casanas-Sanchez V, Perez JA, Fabelo N, Quinto-Alemany D, Diaz ML
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
However, the changes with this particular mix will take place sooner rather than later
The common therapeutic strategy involves iron supplementation (Abu-Ouf & Jan 2015)
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