Lattante, Serena <br/><br/>
TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia.  [electronic resource] 

 -  Neurobiology of aging  Oct 2013 
 - 2443.e1-2 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.2013.04.030  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cohort Studies<br/>Exome--genetics<br/>France--ethnology<br/>Frontotemporal Dementia--ethnology<br/>Humans<br/>Membrane Glycoproteins--genetics<br/>Middle Aged<br/>Mutation<br/>Mutation Rate<br/>Receptors, Immunologic--genetics<br/>White People--genetics