Ohmori, Iori <br/><br/>
CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.  [electronic resource] 

 -  Neurobiology of disease  Feb 2013 
 - 209-17 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1095-953X 
<br/><br/><label>Standard No.: </label>10.1016/j.nbd.2012.10.016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Calcium Channels--genetics<br/>Child<br/>DNA Mutational Analysis<br/>Electroencephalography<br/>Epilepsies, Myoclonic--genetics<br/>Genotype<br/>Humans<br/>Molecular Sequence Data<br/>Patch-Clamp Techniques<br/>Phenotype