Title : Saccadic reaction time and ocular findings in phenylketonuria.

Pub. Date : 2020 May 25

PMID : 32450880






1 Functional Relationships(s)
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1 BACKGROUND: Phenylketonuria (PKU) is an inherited metabolic disorder characterized by reduced activity of phenylalanine hydroxylase resulting in elevated blood phenylalanine (Phe) concentration. Phenylalanine phenylalanine hydroxylase Homo sapiens