A series of simple detection systems for genetic variants of flavin-containing monooxygenase 3 (FMO3) with impaired function in Japanese subjects

Increasing numbers of single-nucleotide substitutions of the human flavin-containing monooxygenase 3 (FMO3) gene are being recorded in mega-databases. Phenotype–gene analyses revealed impaired FMO3 variants associated with the metabolic disorder trimethylaminuria. Here, a series of reliable FMO3 gen...

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Bibliographic Details
Published inDrug metabolism and pharmacokinetics Vol. 41; p. 100420
Main Authors Shimizu, Makiko, Mizugaki, Ami, Koibuchi, Natsumi, Sango, Haruna, Uenuma, Yumi, Yamazaki, Hiroshi
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.12.2021
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Online AccessGet full text
ISSN1347-4367
1880-0920
1880-0920
DOI10.1016/j.dmpk.2021.100420

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