A proteomics approach to further highlight the altered inflammatory condition in Rett syndrome
Author:
Funder
Fondazione Umberto Veronesi
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference87 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
2. Twenty years of surveillance in Rett syndrome: what does this tell us?;Anderson;Orphanet J. Rare Dis.,2014
3. Rett syndrome in Australia: a review of the epidemiology;Laurvick;J. Pediatr.,2006
4. The story of Rett syndrome: from clinic to neurobiology;Chahrour;Neuron,2007
5. Clinical manifestations and stages of Rett syndrome;Hagberg;Ment. Retard. Dev. Disabil. Res. Rev.,2002
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