Blinders, phenotype, and fashionable genetic analysis: A critical examination of the current state of epilepsy genetic studies
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2010.02734.x/fullpdf
Reference44 articles.
1. Mechanisms of seizures and coma in hypoglycemia. Evidence for a direct effect of insulin on electrolyte transport in brain;Arieff;J Clin Invest,1974
2. Astrocytes within multiple sclerosis lesions upregulate sodium channel Nav1.5;Black;Brain,2010
3. Autosomal dominant glut-1 deficiency syndrome and familial epilepsy;Brockmann;Ann Neurol,2001
4. A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy;Cavalleri;Epilepsia,2007
5. De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy;Claes;Hum Mutat,2003
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