Sassi, Celeste <br/><br/>
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.  [electronic resource] 

 -  Neurobiology of aging  Dec 2014 
 - 2881.e1-2881.e6 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.2014.06.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Alzheimer Disease--diagnosis<br/>Amyloid beta-Protein Precursor--genetics<br/>Cohort Studies<br/>Dementia--diagnosis<br/>Diagnosis, Differential<br/>Female<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Genetic Variation--genetics<br/>Humans<br/>Intercellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Middle Aged<br/>Presenilin-1--genetics<br/>Presenilin-2--genetics<br/>Prion Proteins<br/>Prions--genetics<br/>Progranulins<br/>tau Proteins--genetics