Muhle, Hiltrud <br/><br/>
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy.  [electronic resource] 

 -  Epilepsia  Dec 2010 
 - 2453-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-1167 
<br/><br/><label>Standard No.: </label>10.1111/j.1528-1167.2010.02712.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Deaminase--genetics<br/>Adolescent<br/>Chromosomes, Human, Pair 1--genetics<br/>Epilepsy, Absence--diagnosis<br/>Epilepsy, Generalized--genetics<br/>Family<br/>Female<br/>Gene Duplication--genetics<br/>Humans<br/>Male<br/>Pedigree<br/>RNA-Binding Proteins<br/>Receptors, Nicotinic--genetics