The role of oxidative stress in Rett syndrome: an overview

The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting females, is a mutation in the methyl‐CpG binding protein 2 (MeCP2) gene. To date, no cure for RTT exists, although disease reversibility has been demonstrated in animal models. Emerging evidence from...

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Published inAnnals of the New York Academy of Sciences Vol. 1259; no. 1; pp. 121 - 135
Main Authors De Felice, Claudio, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Durand, Thierry, Valacchi, Giuseppe, Ciccoli, Lucia, Hayek, Joussef
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.07.2012
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