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Description
Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)
Its formulated for clean performance, effective fat metabolism, and consistent results
[published correction appears in PLoS One
In addition to being involved in the transport of endogenous (e.g., neurotransmitters) and exogenous (e.g., drugs) substances [178], it also receives carnitine transport [179, 180]
doi: 10.1080/00071660120109980
