Carvill, Gemma L <br/><br/>
GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.  [electronic resource] 

 -  Neurology  Apr 2014 
 - 1245-53 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0000000000000291  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Epilepsies, Myoclonic--genetics<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Munc18 Proteins--genetics<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Receptors, GABA-A--genetics<br/>Young Adult