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Phenylketonuria: A Comprehensive Review of Pathophysiology, Diagnosis, and Management Strategies

Introduction: Phenylketonuria (PKU) is a genetically determined congenital metabolic disorder characterized by the body's inability to properly metabolize the amino acid phenylalanine, which is ingested through food. This deficiency leads to the accumulation of phenylalanine in the blood. If un...

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Main Authors:	Agata Konopka (Author), Zuzanna Szczepaniak (Author), Natalia Wdowiak (Author), Dominika Ziółkowska (Author), Kinga Adamska (Author), Karina Lissak (Author)
Format:	Book
Published:	Nicolaus Copernicus University in Toruń, 2024-08-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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