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Li, V. FMO3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5566 (accessed on 21 September 2026).
Li V. FMO3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5566. Accessed September 21, 2026.
Li, Vivi. "FMO3 Gene" Encyclopedia, https://encyclopedia.pub/entry/5566 (accessed September 21, 2026).
Li, V. (2020, December 25). FMO3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5566
Li, Vivi. "FMO3 Gene." Encyclopedia. Web. 25 December, 2020.
Copy Citation
Flavin containing monooxygenase 3
genes
References
- Bain MA, Fornasini G, Evans AM. Trimethylamine: metabolic, pharmacokinetic andsafety aspects. Curr Drug Metab. 2005 Jun;6(3):227-40. Review.
- Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR. Missensemutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odoursyndrome. Nat Genet. 1997 Dec;17(4):491-4.
- Hernandez D, Addou S, Lee D, Orengo C, Shephard EA, Phillips IR.Trimethylaminuria and a human FMO3 mutation database. Hum Mutat. 2003Sep;22(3):209-13. Review.
- Koukouritaki SB, Poch MT, Henderson MC, Siddens LK, Krueger SK, VanDyke JE,Williams DE, Pajewski NM, Wang T, Hines RN. Identification and functionalanalysis of common human flavin-containing monooxygenase 3 genetic variants. JPharmacol Exp Ther. 2007 Jan;320(1):266-73.
- Krueger SK, Vandyke JE, Williams DE, Hines RN. The role of flavin-containingmonooxygenase (FMO) in the metabolism of tamoxifen and other tertiary amines.Drug Metab Rev. 2006;38(1-2):139-47. Review.
- Mitchell SC. Trimethylaminuria: susceptibility of heterozygotes. Lancet. 1999 Dec 18-25;354(9196):2164-5.
- Zhang J, Tran Q, Lattard V, Cashman JR. Deleterious mutations in theflavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria.Pharmacogenetics. 2003 Aug;13(8):495-500.
- Zhou J, Shephard EA. Mutation, polymorphism and perspectives for the future ofhuman flavin-containing monooxygenase 3. Mutat Res. 2006 Jun;612(3):165-171. doi:10.1016/j.mrrev.2005.09.001.
- Zschocke J, Kohlmueller D, Quak E, Meissner T, Hoffmann GF, Mayatepek E. Mild trimethylaminuria caused by common variants in FMO3 gene. Lancet. 1999 Sep4;354(9181):834-5.
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