Stogmann, E <br/><br/>
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations.  [electronic resource] 

 -  Neurology  Dec 2006 
 - 2029-31 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000250254.67042.1b  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>3' Untranslated Regions--genetics<br/>Adult<br/>Calcium-Binding Proteins--genetics<br/>Epilepsy, Generalized--genetics<br/>Female<br/>Genetic Variation<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Phenotype<br/>Syndrome