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[21] Trimethylaminuria [edit] Trimethylaminuria is an autosomal recessive genetic disorder involving a defect in the function or expression of flavin-containing monooxygenase 3 (FMO3) which results in poor trimethylamine metabolism

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A physical examination with determination of anthropometrical parameters and a complete biochemical analysis was performed before bariatric surgery and at months 1, 3, 6, and 12 following the procedure

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