A long-term follow-up study of Dravet syndrome up to adulthood
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2009.02466.x/fullpdf
Reference38 articles.
1. SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy;Buoni;Neurology,2006
2. Dravet syndrome: a study of 53 patients;Caraballo;Epilepsy Res,2006
3. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
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