Clinical utility gene card for: Trimethylaminuria – update 2014
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2014226.pdf
Reference46 articles.
1. Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR : Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome. Nat Genet 1997; 17: 491–494.
2. Treacy EP, Akerman BR, Chow LML et al. Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication. Hum Mol Genet 1998; 7: 839–845.
3. Fujieda M, Yamazaki H, Togashi M, Saito T, Kamataki T : Two novel single nucleotide polymorphisms (SNPs) of the FMO3 gene in Japanese. Drug Metab Pharmacokinet 2003; 18: 333–335.
4. Yamazaki H, Fujita H, Gunji T et al. Stop codon mutations in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population. Mol Genet Metab 2007; 90: 58–63.
5. Motika MS, Zhang J, Zheng X, Riedler K, Cashman JR : Novel variants of the human flavin-containing monooxygenase 3 (FMO3) gene associated with trimethylaminuria. Mol Genet Metab 2009; 97: 128–135.
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