Inflammatory Lung Disease in Rett Syndrome

Rett syndrome (RTT) is a pervasive neurodevelopmental disorder mainly linked to mutations in the gene encoding the methyl-CpG-binding protein 2 (MeCP2). Respiratory dysfunction, historically credited to brainstem immaturity, represents a major challenge in RTT. Our aim was to characterize the relati...

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Detalhes bibliográficos
Main Authors: De Felice, Claudio, Rossi, Marcello, Leoncini, Silvia, Chisci, Glauco, Signorini, Cinzia, Lonetti, Giuseppina, Vannuccini, Laura, Spina, Donatella, Ginori, Alessandro, Iacona, Ingrid, Cortelazzo, Alessio, Pecorelli, Alessandra, Valacchi, Giuseppe, Ciccoli, Lucia, Pizzorusso, Tommaso, Hayek, Joussef
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
Assuntos:
Clinical Study
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3976920/
https://ncbi.nlm.nih.gov/pubmed/24757286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/560120
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