The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of intervention

BACKGROUND: Cystic fibrosis (CF) is caused by mutations in the CFTR gene that predispose the airway to infection. Chronic infection by pathogens such as Pseudomonas aeruginosa leads to inflammation that gradually degrades lung function, resulting in morbidity and early mortality. In a previous study...

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Autori principali: Hampton, Thomas H, Green, Deanna M, Cutting, Garry R, Morrison, Hilary G, Sogin, Mitchell L, Gifford, Alex H, Stanton, Bruce A, O’Toole, George A
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2014
Soggetti:
Short Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4113139/
https://ncbi.nlm.nih.gov/pubmed/25071935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2049-2618-2-14
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