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Food Regime for Phenylketonuria: Presenting Complications and Possible Solutions
In the category of rare inherited genetic disorders, phenylketonuria is a prominent example. Here, the defective phenylalanine hydroxylase enzyme fails to catalyze conversion of phenylalanine to tyrosine. This leads to not only excess deposition of phenylalanine leading to phenylalanine toxicity but...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785131/ https://www.ncbi.nlm.nih.gov/pubmed/35082498 http://dx.doi.org/10.2147/JMDH.S330845 |