Mild trimethylaminuria caused by common variants in FM03 gene

@article{Zschocke1999MildTC,
  title={Mild trimethylaminuria caused by common variants in FM03 gene},
  author={J. Zschocke and D. Kohlmueller and E. Quak and T. Meissner and E. Mayatepek},
  journal={The Lancet},
  year={1999},
  volume={354},
  pages={834-835}
}
  • J. Zschocke, D. Kohlmueller, +2 authors E. Mayatepek
  • Published 1999
  • Medicine
  • The Lancet
  • Mild to transient trimethylaminuria is caused by common variants in the FMO3 gene leading to greatly reduced enzyme activity in vivo. FMO3 deficiency may have clinical relevance well beyond unpleasant body odour. 
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    References

    SHOWING 1-4 OF 4 REFERENCES