Schellenberg, G D <br/><br/>
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.  [electronic resource] 

 -  American journal of human genetics  Sep 1991 
 - 511-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Alzheimer Disease--genetics<br/>Amyloid beta-Peptides--genetics<br/>Amyloid beta-Protein Precursor<br/>Amyloidosis--genetics<br/>Base Sequence<br/>Chromosomes, Human, Pair 21<br/>Down Syndrome--genetics<br/>Europe--epidemiology<br/>Female<br/>Humans<br/>Lod Score<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>PrPC Proteins<br/>Protein Precursors--genetics<br/>Viral Proteins--genetics