Protein substitutions as new-generation pharmanutrition approach to managing phenylketonuria
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 phenylalanine (Phe) blood concentrations (hyperphenylalaninemia) that harm the...
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| Main Authors: | , , , |
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| Format: | Book |
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The Korean Pediatric Society,
2023-08-01T00:00:00Z.
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