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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...
Gorde:
| Argitaratua izan da: | Redox Rep |
|---|---|
| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Taylor & Francis
2013
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| Gaiak: | |
| Sarrera elektronikoa: | 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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