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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918959/
https://www.ncbi.nlm.nih.gov/pubmed/27336782
http://dx.doi.org/10.1371/journal.pone.0157513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918959/
https://www.ncbi.nlm.nih.gov/pubmed/27336782
http://dx.doi.org/10.1371/journal.pone.0157513

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