Ghanim, Mustapha <br/><br/>
CHMP2B mutations are rare in French families with frontotemporal lobar degeneration.  [electronic resource] 

 -  Journal of neurology  Dec 2010 
 - 2032-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1459 
<br/><br/><label>Standard No.: </label>10.1007/s00415-010-5655-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Endosomal Sorting Complexes Required for Transport--genetics<br/>Female<br/>Frontotemporal Lobar Degeneration--diagnosis<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Phenotype