Cochran, J Nicholas <br/><br/>
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles.  [electronic resource] 

 -  Cold Spring Harbor molecular case studies  12 2019 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2373-2873 
<br/><br/><label>Standard No.: </label>10.1101/mcs.a003491  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alleles<br/>Alzheimer Disease--genetics<br/>Apolipoprotein E4--genetics<br/>Base Sequence<br/>C9orf72 Protein--genetics<br/>Chromosome Mapping<br/>Dementia--genetics<br/>Female<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Genome-Wide Association Study<br/>Humans<br/>Male<br/>Middle Aged<br/>Odds Ratio<br/>Penetrance<br/>Risk Factors<br/>Whole Genome Sequencing--methods