Peng, Xiang-Lei <br/><br/>
Novel APP K724M mutation causes Chinese early-onset familial Alzheimer's disease and increases amyloid-β42 to amyloid-β40 ratio.  [electronic resource] 

 -  Neurobiology of aging  Nov 2014 
 - 2657.e1-2657.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.2014.06.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Alzheimer Disease--genetics<br/>Amyloid beta-Peptides--metabolism<br/>Amyloid beta-Protein Precursor--genetics<br/>Asian People--genetics<br/>Female<br/>Genetic Association Studies<br/>HEK293 Cells<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Peptide Fragments--metabolism