Phenylketonuria and Gut Microbiota: A Controlled Study Based on Next-Generation Sequencing

Phenylketonuria (PKU) is an inborn error of metabolism associated with high blood levels of phenylalanine (Phe). A Phe-restricted diet supplemented with L-amino acids is the main treatment strategy for this disease; if started early, most neurological abnormalities can be prevented. The healthy huma...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Pinheiro de Oliveira, Felipe, Mendes, Roberta Hack, Dobbler, Priscila Thiago, Mai, Volker, Pylro, Victor Salter, Waugh, Sheldon G, Vairo, Filippo, Refosco, Lilia Farret, Roesch, Luiz Fernando Würdig, Schwartz, Ida Vanessa Doederlein
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4918959/
https://ncbi.nlm.nih.gov/pubmed/27336782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0157513
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