A Plasma Proteomic Approach in Rett Syndrome: Classical versus Preserved Speech Variant

Rett syndrome (RTT) is a progressive neurodevelopmental disorder mainly caused by mutations in the gene encoding the methyl-CpG-binding protein 2 (MeCP2). Although over 200 mutations types have been identified so far, nine of which the most frequent ones. A wide phenotypical heterogeneity is a well-...

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Detalles Bibliográficos
Autores principales: Cortelazzo, Alessio, Guerranti, Roberto, De Felice, Claudio, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Landi, Claudia, Bini, Luca, Montomoli, Barbara, Sticozzi, Claudia, Ciccoli, Lucia, Valacchi, Giuseppe, Hayek, Joussef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884802/
https://www.ncbi.nlm.nih.gov/pubmed/24453418
http://dx.doi.org/10.1155/2013/438653

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