Management precautions for risk of obesity are necessary among infants with PKU carrying the rs113883650 variant of the LAT1 gene: A cross-sectional study
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DOI: 10.1371/journal.pone.0264084
Abstract: Patients with phenylketonuria (PKU), an inborn error of phenylalanine metabolism, require consistent treatment to avoid the brain toxicity caused by hyperphenylalaninemia. The treatment consists of life-long use of a low-phenylalanine diet, which aims at decreasing… read more here.
Keywords: variant lat1; phenylalanine; infants pku; rs113883650 variant ... See more keywords