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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Published in | Drug metabolism and pharmacokinetics Vol. 41; p. 100420 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.12.2021
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Subjects | |
Online Access | Get full text |
ISSN | 1347-4367 1880-0920 1880-0920 |
DOI | 10.1016/j.dmpk.2021.100420 |
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