Plasma phospholipidome analysis reveals a different profile between children with phenylketonuria and healthy children

Phenylketonuria (PKU) is the most prevalent innate error in amino acid metabolism. PKU is characterized by the deficiency of a phenylalanine (Phe) metabolism enzyme, phenylalanine hydroxylase, which is responsible for the conversion of Phe into tyrosine (Tyr). Deficiency of this enzyme causes the ac...

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Bibliographic Details
Main Author: Guerra, Inês Maria dos Santos (author)
Format: masterThesis
Language:eng
Published: 2022
Subjects:
Inborn error of metabolism
Phenylketonuria
Lipid changes
Oxidative stress
Lipidomics
Mass spectrometry
Online Access:http://hdl.handle.net/10773/30612
Country:Portugal
Oai:oai:ria.ua.pt:10773/30612

Internet

http://hdl.handle.net/10773/30612

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