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Published in 2022 at "Journal of medicinal food"
DOI: 10.1089/jmf.2021.0111
Abstract: Phenylketonuria (PKU) is an autosomal recessive disease caused by variants in the gene that encodes phenylalanine hydroxylase (PAH), limiting the metabolism of phenylalanine (Phe). When PAH activity is absent or hindered, Phe is not converted…
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Keywords:
phenylalanine;
integrative review;
consumption fruits;
metabolic control ... See more keywords