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- W978641683 abstract "Phenylketonuria (PKU) is an inherited inborn error of phenylalanine (PHE) metabolism caused by deficiency of the hepatic enzyme, phenylalanine hydroxyls (PAH). Therefore PHE accumulates in plasma l..." @default.
- W978641683 created "2016-06-24" @default.
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- W978641683 date "2015-04-01" @default.
- W978641683 modified "2023-09-23" @default.
- W978641683 title "Protein Requirements in Children with Phenylketonuria (PKU)" @default.
- W978641683 doi "https://doi.org/10.1096/fasebj.29.1_supplement.742.9" @default.
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