Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals

Phenylketonuria (PKU) is an inherited metabolic disorder derived from a deficiency in the enzyme phenylalanine hydroxylase, which converts the amino acid phenylalanine (Phe) into tyrosine (Tyr). Here we aimed to examine the metabolism of Phe and Tyr in heterozygotes for PKU during fasting and after...

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Principais autores:	Roseani Andrade MSc, Vaneisse Monteiro MSc, Cléber Cruz MSc, Carla Silva BS, Adriana Bastos MSc, Luiz Silva PhD
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT) 2015-04-01
סדרה:	Journal of Inborn Errors of Metabolism and Screening
גישה מקוונת:	https://doi.org/10.1177/2326409815573962
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!