Postnatal Loss of Methyl-CpG Binding Protein 2 in the Forebrain is Sufficient to Mediate Behavioral Aspects of Rett Syndrome in Mice
Author:
Publisher
Elsevier BV
Subject
Biological Psychiatry
Reference25 articles.
1. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes;Amir;Ann Neurol,2000
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
3. The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin;Auerbach;Hum Mol Genet,2001
4. Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA;Ballestar;Biochemistry,2000
5. MECP2 mutations account for most cases of typical forms of Rett syndrome;Bienvenu;Hum Mol Genet,2000
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