Chatron, Nicolas <br/><br/>
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant.  [electronic resource] 

 -  Annals of neurology  05 2018 
 - 926-934 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>1531-8249 
<br/><br/><label>Standard No.: </label>10.1002/ana.25222  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>DNA-Binding Proteins--genetics<br/>Databases, Genetic<br/>Electroencephalography--methods<br/>Epilepsies, Myoclonic--genetics<br/>Epilepsy, Absence--genetics<br/>Female<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Infant<br/>Male<br/>Phenotype<br/>Seizures--genetics<br/>Young Adult