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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3884802/
https://ncbi.nlm.nih.gov/pubmed/24453418
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/438653
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