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

Overview of attention for article published in Journal of Inborn Errors of Metabolism and Screening, April 2015

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Nutrición 360, 17 Jun 2015

La fenilcetonuria ( PKU) es un trastorno metabólico hereditario derivada de una deficiencia en la enzima fenilalanina…

FARMACOMED S.A.C., 17 Jun 2015

La fenilcetonuria ( PKU) es un trastorno metabólico hereditario derivada de una deficiencia en la enzima fenilalanina…

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