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Abstract Trimethylaminuria (TMAU), also known as fish odor syndrome, is a rare metabolic disorder resulting from a deficiency in the enzyme flavin-containing monooxygenase 3, which is responsible for the detoxification of trimethylamine produced during the metabolism of certain foods

In this section twelve mice were divided into four groups (0d, 1d, 3d and 7d) with 3 mice in each group