Le Ber, Isabelle <br/><br/>
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes.  [electronic resource] 

 -  Neurobiology of aging  Apr 2014 
 - 934.e5-6 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.2013.09.016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyotrophic Lateral Sclerosis--genetics<br/>Cohort Studies<br/>Frontotemporal Lobar Degeneration--genetics<br/>Heterogeneous Nuclear Ribonucleoprotein A1<br/>Heterogeneous-Nuclear Ribonucleoprotein Group A-B--genetics<br/>Mutation<br/>Myositis, Inclusion Body--genetics<br/>Osteitis Deformans--genetics