Heron, Sarah E <br/><br/>
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.  [electronic resource] 

 -  Epilepsia  May 2013 
 - e86-9 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.12167  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age Factors<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Infant<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Phenotype<br/>Spasms, Infantile--genetics