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Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia.
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Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria.
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Kinetics of phenylalanine disappearance after intravenous load in phenylketonuria and its genetic variants.
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Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants.
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1
Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria.
Proc Natl Acad Sci U S A. 1973 Feb;70(2):552-6. doi: 10.1073/pnas.70.2.552.

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