Oxidative stress in Rett syndrome: Natural history, genotype, and variants

Objectives Rett syndrome (RTT) is an X-linked autism spectrum disorder caused by mutations in the MeCP2 gene in the great majority of cases. Evidence suggests a potential role of oxidative stress (OS) in its pathogenesis. Here, we investigated the potential value of OS markers (non-protein-bound iro...

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Detalhes bibliográficos
Publicado no:Redox Rep
Main Authors: Leoncini, Silvia, De Felice, Claudio, Signorini, Cinzia, Pecorelli, Alessandra, Durand, Thierry, Valacchi, Giuseppe, Ciccoli, Lucia, Hayek, Joussef
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6837451/
https://ncbi.nlm.nih.gov/pubmed/21888765
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1179/1351000211Y.0000000004
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