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Phenylketonuria (PKU) is a genetic disorder caused by a deficiency in the enzyme phenylalanine hydroxylase (PAH). This enzyme is responsible for converting the amino acid phenylalanine into tyrosine, another amino acid. In individuals with PKU, the inability _______ ____ _________ _______ ___ _____ _________ ______ ____ ___ _______ _________.
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