The genetics of Dravet syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.02997.x/fullpdf
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1. Epileptogenic channelopathies: experimental models of human pathologies;Avanzini;Epilepsia,2007
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3. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
4. Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancy;Depienne;Hum Mutat,2006
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