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Article

Deleterious mutations in the flavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria.

Pharmacogenetics - 1 Aug 2003

Zhang Jun, Tran Quyen, Lattard Virginie, Cashman John R

Abstract excerpt

The primary genetic form of trimethylaminuria (TMAU) is caused by inherited defects in the flavin-containing monooxygenase 3 (FMO3) gene. Defective FMO3 has a decreased ability to catalyze the N-oxygenation of the dietary-derived malodourous amine, trimethylamine. We report two novel deleterious...

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Source

Identifiers

PMID: 12893987
DOI: 10.1097/00008571-200308000-00007

Genes

FMO3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12893987-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Deleterious mutations in the flavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria.PMID 12893987Read ↗

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