References
- Rubinstein M Han S Tai C Westenbroek RE Hunker A Scheuer T Dissecting the phenotypes of Dravet syndrome by gene deletion Brain 2015 Aug 138 Pt 8 2219 33 10.1093/brain/awv142 26017580
- Wu YW Sullivan J McDaniel SS Meisler MH Walsh EM Li SX Incidence of Dravet Syndrome in a US Population Pediatrics 2015 Nov 136 5 e1310 5 10.1542/peds.2015-1807 26438699
-
Fujiwara
T
Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies
Epilepsy Res
2006
Aug
70
Suppl 1 S223 30 10.1016/j.eplepsyres.2006.01.019 16806826 - Meisler MH O’Brien JE Sharkey LM Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects J Physiol 2010 Jun 588 Pt 11 1841 8 10.1113/jphysiol.2010.188482 20351042
- Battaglia D Ricci D Chieffo D Guzzetta F Outlining a core neuropsychological phenotype for Dravet syndrome Epilepsy Res 2016 Feb 120 91 7 10.1016/j.eplepsyres.2015.11.020 26808204
DOI: https://doi.org/10.15844/pedneurbriefs-30-5-1 | Journal eISSN: 2166-6482
Language: English
Page range: 28 - 28
Submitted on: Aug 21, 2016
Accepted on: Aug 27, 2016
Published on: Aug 30, 2016
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2016 Rebecca Garcia-Sosa, Linda C. Laux, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.
