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Description
It acts as a transporter, moving fatty acids into the mitochondria to be burned for fuel
Key takeaways: Trimethylaminuria (TMAU) is caused by mutations in the FMO3 gene, leading to high levels of trimethylamine (TMA) with a distinctive odor
Dietary precursors of trimethylamine in man: a pilot study
Diet is known to have an important impact on health and disease
Pourquoi prendre de la L-carnitine
Significance of renal gamma-butyrobetaine hydroxylase for carnitine biosynthesis in man
