Epilepsy in Rett syndrome, andCDKL5- andFOXG1-gene-related encephalopathies
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2012.03656.x/fullpdf
Reference96 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
2. CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients;Archer;J Med Genet,2006
3. Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X- chromosome inactivation;Archer;J Med Genet,2007
4. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;Am J Hum Genet,2008
5. Neuropathology of Rett syndrome;Armstrong;J Child Neurol,2005
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