Schubert, Julian <br/><br/>
PRRT2 mutations are the major cause of benign familial infantile seizures.  [electronic resource] 

 -  Human mutation  Oct 2012 
 - 1439-43 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.22126  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Humans<br/>Infant<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Pedigree<br/>Seizures, Febrile--genetics<br/>Spasms, Infantile--genetics