Howell, Katherine B <br/><br/>
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.  [electronic resource] 

 -  Neurology  Sep 2015 
 - 958-66 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.0000000000001926  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Brain Diseases--complications<br/>Child<br/>Child, Preschool<br/>Electroencephalography--methods<br/>Epilepsies, Partial--complications<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Infant<br/>Male<br/>Mutation--genetics<br/>NAV1.2 Voltage-Gated Sodium Channel--genetics<br/>Phenotype<br/>Seizures--complications<br/>Spasms, Infantile--genetics<br/>Young Adult