Author:
De Felice Claudio,Ciccoli Lucia,Leoncini Silvia,Signorini Cinzia,Rossi Marcello,Vannuccini Laura,Guazzi Gianni,Latini Giuseppe,Comporti Mario,Valacchi Giuseppe,Hayek Joussef
Subject
Physiology (medical),Biochemistry
Reference61 articles.
1. Uber ein eigartiges hirnatrophisches Syndrom bei Hyperammoniamie in Kindesalter;Rett;Wien Med. Wochenschr.,1966
2. progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls. Rett's syndrome: report of 35 cases;Hagberg;Ann. Neurol.,1983
3. The story of Rett syndrome: from clinic to neurobiology;Chahrour;Neuron,2007
4. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
5. MeCP2, a key contributor to neurological disease, activates and represses transcription;Chahrour;Science,2008
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