Trimethylaminuria: susceptibility of heterozygotes
- PMID: 10609842
- DOI: 10.1016/s0140-6736(05)77067-7
Trimethylaminuria: susceptibility of heterozygotes
Comment on
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Mild trimethylaminuria caused by common variants in FMO3 gene.Lancet. 1999 Sep 4;354(9181):834-5. doi: 10.1016/s0140-6736(99)80019-1. Lancet. 1999. PMID: 10485731
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