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MMA is a genetically heterogeneous disorder, with the majority (~60%) of cases caused by complete ( mut 0 ) or partial ( mut ) deficiency of the enzyme methylmalonyl-CoA mutase (MMUT) and the remainder due to errors in the synthesis or transport of 5-deoxyadenosylcobalamin, a vitamin B 12 derivative and essential cofactor of the reaction (1, 2)

The goal is a stronger and more complete recovery

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But it still provides the same thyroid-balancing, antibody-lowering benefits regardless of whatever condition you may have

Chair in Surgery, and colleagues previously showed that GPX7, a member of the glutathione peroxidase family of antioxidant enzymes, is often silenced or lost in Barretts esophagus and esophageal cancer