A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.03059.x/fullpdf
Reference26 articles.
1. Epilepsies in twins: genetics of the major epilepsy syndromes;Berkovic;Ann Neurol,1998
2. Childhood absence epilepsy: behavioral, cognitive, and linguistic comorbidities;Caplan;Epilepsia,2008
3. Association between genetic variation of CACNA1H and childhood absence epilepsy;Chen;Ann Neurol,2003
4. Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14;Chioza;Epilepsy Res,2009
5. Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy;Cossette;Nat Genet,2002
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