Urine Phenylacetylglutamine Determination in Patients with Hyperphenylalaninemia

Phenylketonuria (PKU), an autosomal-recessive inborn error of phenylalanine (Phe) metabolism is the most prevalent disorder of amino acid metabolism. Currently, clinical follow-up relies on frequent monitoring of Phe levels in blood. We hypothesize that the urine level of phenylacetylglutamine (PAG)...

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Detalles Bibliográficos
Autores principales: Andrade, Fernando, Cano, Ainara, Unceta Suarez, María, Arza, Arantza, Vinuesa, Ana, Ceberio, Leticia, López-Oslé, Nuria, de Frutos, Gorka, López-Oceja, Raquel, Aznal, Elena, González-Lamuño, Domingo, de las Heras, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396897/
https://www.ncbi.nlm.nih.gov/pubmed/34441968
http://dx.doi.org/10.3390/jcm10163674

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396897/
https://www.ncbi.nlm.nih.gov/pubmed/34441968
http://dx.doi.org/10.3390/jcm10163674

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