Electrographic and pharmacological characterization of a progressive epilepsy phenotype in female MeCP2-deficient mice
Author:
Funder
Canadian Institutes of Health Research
International Rett Syndrome Foundation
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference46 articles.
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2. Parental view of epilepsy in Rett Syndrome;Bahi-Buisson;Brain Dev.,2008
3. Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging;Calfa;J. Neurophysiol.,2011
4. Epilepsy in Rett syndrome: association between phenotype and genotype, and implications for practice;Cardoza;Seizure,2011
5. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice;Chen;Nat. Genet.,2001
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