Lal, Dennis <br/><br/>
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.  [electronic resource] 

 -  PloS one  2016 
 - e0150426 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0150426  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Case-Control Studies<br/>Epilepsy--epidemiology<br/>Female<br/>Humans<br/>Male<br/>Mutation, Missense<br/>NAV1.1 Voltage-Gated Sodium Channel--genetics<br/>Risk Factors<br/>Syndrome