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Individuals with the milder forms of VLCADD usually have mutations that cause only a partial reduction of the enzymes function.[ref] Inheritance of VLCADD: VLCADD is an autosomal recessive condition, meaning that you need two mutations (one from each parent) to have it

- Promotes antioxidant protection throughout the nervous system

Rat digestion is different from humans, and a fecal analysis doesnt take into account that bacteria in the colon can change the amino acid composition of the feces

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