Persistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett Syndrome

Rett syndrome (RTT) is a rare neurodevelopmental disorder usually caused by mutations in the X-linked gene methyl-CpG-binding protein 2 (MECP2). Several Mecp2 mutant mouse lines have been developed recapitulating part of the clinical features. In particular, Mecp2-308 female heterozygous mice, beari...

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Detalles Bibliográficos
Autores principales: Cortelazzo, Alessio, De Felice, Claudio, De Filippis, Bianca, Ricceri, Laura, Laviola, Giovanni, Leoncini, Silvia, Signorini, Cinzia, Pescaglini, Monica, Guerranti, Roberto, Timperio, Anna Maria, Zolla, Lello, Ciccoli, Lucia, Hayek, Joussef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448068/
https://www.ncbi.nlm.nih.gov/pubmed/28592917
http://dx.doi.org/10.1155/2017/9467819

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448068/
https://www.ncbi.nlm.nih.gov/pubmed/28592917
http://dx.doi.org/10.1155/2017/9467819

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