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R NAT2 is the more clinically relevant because it metabolizes the majority of amine drugs (isoniazid, hydralazine, procainamide, sulfonamides, caffeine)

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The nascent apoB100 is then partially lapidated to form a lipid-poor primordial VLDL particle, which is facilitated by microsomal triglyceride transfer protein (MTP)

identified a deletion in exon 2 of the X-linked trimethyl lysine hydroxylase gene ( TMLHE ), which encodes the enzyme catalyzing the first step in L-carnitine synthesis, in an individual with autism 6

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