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hyperphenylalaninemia, non-pku mild
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PAH
In vitro expression analysis of mutations in phenylalanine hydroxylase: linking genotype to phenotype and structure to function
How PAH gene mutations cause hyper-phenylalaninemia and why mechanism matters: insights from in vitro expression
Tetrahydropterin-dependent amino acid hydroxylases
A new cofactor required for the enzymatic conversion of phenylalanine to tyrosine
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