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Emergencias 30 , 9197 (2018)
Karnitin eksiklii, hcreye karnitin getiren proteindeki genetik bir mutasyon (gen kusuru) (birincil karnitin eksiklii) veya dier metabolik hastalklar (ikincil karnitin eksiklii) sonucu ortaya kabilir
doi: 10.1136/bmj.38169.486701.7C
However, in trimethylaminuria (TMAU), a rare genetic disorder, deficient FMO3 leads to TMA accumulation and body odor
In contrast, CRC exhibits low expression level of OCTN2 [28]
