Genetic basis of the human epilepsies
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference20 articles.
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2. Germline mutations in the homobox gene EMX2 in patients with severe schizencephaly;Brunelli;Nat. Genet.,1996
3. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family;Charlier;Nat. Genet.,1998
4. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome;Des Portes;Cell,1998
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1. Computational Neurogenetic Modeling: Gene-Dependent Dynamics of Cortex and Idiopathic Epilepsy;Springer Handbook of Bio-/Neuroinformatics;2014
2. Dentate gyrus network dysfunctions precede the symptomatic phase in a genetic mouse model of seizures;Frontiers in Cellular Neuroscience;2013
3. Rat Genome Mapping and Genomics;Genome Mapping and Genomics in Laboratory Animals;2012
4. Role of voltage-gated calcium channels in epilepsy;Pflügers Archiv - European Journal of Physiology;2009-12-20
5. Modeling brain dynamics using computational neurogenetic approach;Cognitive Neurodynamics;2008-09-16
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