Analysis of six novel flavin-containing monooxygenase 3 (FMO3) gene variants found in a Japanese population suffering from trimethylaminuria
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference18 articles.
1. Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome;Dolphin;Nat. Genet.,1997
2. A novel mutation in the flavin-containing monooxygenase 3 gene (FMO3) of a Norwegian family causes trimethylaminuria;Allerston;Mol. Gen. Genomics.,2009
3. Variants in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population;Shimizu;Mol. Genet. Metab.,2012
4. Relationships between flavin-containing monooxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population;Shimizu;Br. J. Clin. Pharmacol.,2014
5. Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort;Akerman;Mol. Genet. Metab.,1999
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1. Variants of Flavin-Containing Monooxygenase 3 Found in Subjects in an Updated Database of Genome Resources;Drug Metabolism and Disposition;2023-04-11
2. Further survey of genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects found in an updated database of genome resources and identified by phenotyping for trimethylaminuria;Drug Metabolism and Pharmacokinetics;2022-10
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4. A series of simple detection systems for genetic variants of flavin-containing monooxygenase 3 (FMO3) with impaired function in Japanese subjects;Drug Metabolism and Pharmacokinetics;2021-12
5. Genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects identified by phenotyping for trimethylaminuria and found in a database of genome resources;Drug Metabolism and Pharmacokinetics;2021-06
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