Daoud, Hussein <br/><br/>
UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.  [electronic resource] 

 -  Neurobiology of aging  Sep 2012 
 - 2230.e1-2230.e5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1558-1497 
<br/><br/><label>Standard No.: </label>10.1016/j.neurobiolaging.2012.03.015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Animals<br/>Autophagy-Related Proteins<br/>Canada<br/>Cell Cycle Proteins--genetics<br/>Computational Biology<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Mutation, Missense--genetics<br/>Ubiquitins--genetics<br/>White People--genetics