Biomarkers
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This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]
Bayer
University of Kansas Medical Center
University of Miami
Russian Cardiology Research and Production Center
Insmed Incorporated
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Clinical Intelligence Agent
Scientific Literature Agent
5 papers
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