Associated Papers
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes.
Alibrandi S et al.
Molecules (basel, Switzerland), 2021
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation.
Scimone C et al.
Journal of Digestive Diseases, 2016
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.
D'Angelo R et al.
Journal of Medical Case Reports, 2014
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.
Treacy EP et al.
Human Molecular Genetics, 1998
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