One of the most prominent researchers into flavin mono oxygenase enzymes (and trimethylaminuria) is Dr Cashman at the HBRI in San Diego.
The HBRI is kind enough to allow DNA testing for TMAU associated mutants without a doctor's prescription for $400.
http://www.hbri.org/TMAuria.htm
It is a charity and accepts donations for trimethylaminuria research, although it is unclear if a donation goes exclusively towards TMAU research. Perhaps this can be clarified later. Anyone interested should contact the HBRI direct.
This is posted only to promote awareness. The accuracy of the information cannot be taken as completely correct at this point. This means that in the USA, if someone chooses to test for trimethylaminuria on their own, they can do the urine test via The Denver Hospital once their lab is operating again, and can do the DNA test via the HBRI (although it presumably involves someone drawing the blood sample).
If there are any inaccuracies in this post, please let us know
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