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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| Principais autores: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Korean Pediatric Society
2023-08-01
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| Serier: | Clinical and Experimental Pediatrics |
| Fag: | |
| Online adgang: | http://www.e-cep.org/upload/pdf/cep-2022-00584.pdf |
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