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SSADH deficiency is a rare autosomal genetic disease affecting a key enzyme in the catabolism of GABA in which patients exhibit different symptoms, including ataxia, hypotonia, communication deficits and intellectual disability

In contrast, a study by Li et al

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zel et al

Research has indicated that mitochondrial GSTs in humans play important roles in the detoxification of lipid peroxide and lipid metabolism [61]

Many formulations add vitamin B12 (cyanocobalamin) , which is where the MIC B12 or lipo MIC naming comes from