van der Zee, Julie <br/><br/>
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.  [electronic resource] 

 -  Acta neuropathologica  Sep 2014 
 - 397-410 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-0533 
<br/><br/><label>Standard No.: </label>10.1007/s00401-014-1298-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing--genetics<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amyotrophic Lateral Sclerosis<br/>Animals<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Europe<br/>Female<br/>Frontotemporal Lobar Degeneration--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>International Cooperation<br/>Male<br/>Meta-Analysis as Topic<br/>Middle Aged<br/>Polymorphism, Single Nucleotide--genetics<br/>Sequestosome-1 Protein