Early-onset behavioral and neurochemical deficits in the genetic mouse model of phenylketonuria

Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenylalanine hydroxylase deficiency, leading to high phenylalanine and low tyrosine levels in blood and brain causing profound cognitive disability, if untreated. Since 1960, population is screened for hype...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Fiori, Elena, Oddi, Diego, Ventura, Rossella, Colamartino, Marco, Valzania, Alessandro, D’Amato, Francesca Romana, Bruinenberg, Vibeke, van der Zee, Eddy, Puglisi-Allegra, Stefano, Pascucci, Tiziana
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5574541/
https://ncbi.nlm.nih.gov/pubmed/28850618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0183430
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