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Protein substitutions as new-generation pharmanutrition approach to managing phenylketonuria

Keskin FN, Şahin TÖ, Capasso R, Ağagündüz D

Phenylketonuria (PKU), an autosomal recessive inherited metabolic disorder, is caused by a mutation in the phenylalanine hydroxylase (PAH) gene on the 12th chromosome. Defective PAH activity ultimately leads to increased...
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