Lal, Dennis <br/><br/>
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.  [electronic resource] 

 -  Epilepsia  Sep 2015 
 - e129-33 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-1167 
<br/><br/><label>Standard No.: </label>10.1111/epi.13076  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Epilepsies, Partial--genetics<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Meta-Analysis as Topic<br/>Middle Aged<br/>Phenotype<br/>RNA Splicing Factors<br/>RNA-Binding Proteins--genetics<br/>Sequence Deletion--genetics