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Phenylalanine is an essential aromatic amino acid that serves as a building block for proteins and a precursor for several important biomolecules, including tyrosine, dopamine, norepinephrine, epinephrine, melanin, and phenethylamine. It plays a critical role in protein synthesis and neurotransmitter production. However, individuals with phenylketonuria (PKU) must strictly limit phenylalanine intake due to a deficiency in the enzyme phenylalanine hydroxylase, which can lead to toxic accumulation of phenylalanine and neurological damage.
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