Title : Aptamer-based assay for monitoring genetic disorder phenylketonuria (PKU).

Pub. Date : 2018 Sep

PMID : 29777816






1 Functional Relationships(s)
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Protein Name
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1 The genetic disorder phenylketonuria (PKU) is the inability to metabolize phenylalanine because of a lack of the enzyme phenylalanine hydroxylase. Phenylalanine phenylalanine hydroxylase Homo sapiens