Boissé Lomax, Lysa <br/><br/>
'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation.  [electronic resource] 

 -  Brain : a journal of neurology  Apr 2013 
 - 1146-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awt021  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Ataxia--genetics<br/>Child<br/>Electroencephalography<br/>Europe<br/>Female<br/>Humans<br/>Male<br/>Mutation--genetics<br/>Myoclonic Epilepsies, Progressive--genetics<br/>North Sea<br/>Phenotype<br/>Qb-SNARE Proteins--genetics<br/>Young Adult