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Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort

✍ Scribed by B.R. Akerman; H. Lemass; L.M.L. Chow; D.M. Lambert; C. Greenberg; C. Bibeau; O.A. Mamer; E.P. Treacy


Book ID
115639569
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
76 KB
Volume
68
Category
Article
ISSN
1096-7192

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The mammalian flavin-containing monooxygenases catalyze the NADPH-dependent N-oxygenation of nucleophilic nitrogen-, sulfur-, and phosphorus-containing chemicals, drugs, and xenobiotics, including trimethylamine. The FMO3 gene encodes the dominant catalytically active isoform present in human liver.