Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome

Author:

Filosa Stefania,Pecorelli Alessandra,D'Esposito Maurizio,Valacchi Giuseppe,Hajek Joussef

Publisher

Elsevier BV

Subject

Physiology (medical),Biochemistry

Reference163 articles.

1. The story of Rett syndrome: from clinic to neurobiology;Chahrour;Neuron,2007

2. Rett syndrome in Australia: a review of the epidemiology;Laurvick;J Pediatr.,2006

3. [On a unusual brain atrophy syndrome in hyperammonemia in childhood];Rett;Wien Med Wochenschr,1966

4. Clinical manifestations and stages of Rett syndrome;Hagberg;Ment Retard Dev Disabil Res Rev,2002

5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet.,1999

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