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This means a person must have two mutated FMO3 genes, one from each parent, to develop the condition

10.1007/s10545-009-1126-8 40 TajimaG.HaraK.TsumuraM.KagawaR.OkadaS.SakuraN.et al (2017)

J., and DeFelice, S

Jun 18 2019;139(25):2892-2909
