Behr, Elijah R <br/><br/>
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.  [electronic resource] 

 -  Cardiovascular research  Jun 2015 
 - 520-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1755-3245 
<br/><br/><label>Standard No.: </label>10.1093/cvr/cvv042  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials<br/>Adult<br/>Aged<br/>Brugada Syndrome--diagnosis<br/>Case-Control Studies<br/>Cell Line<br/>Computational Biology<br/>DNA Mutational Analysis<br/>Databases, Genetic<br/>Europe<br/>Female<br/>Gene Frequency<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Heredity<br/>Humans<br/>Male<br/>Middle Aged<br/>NAV1.8 Voltage-Gated Sodium Channel--genetics<br/>Odds Ratio<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Risk Factors<br/>Saudi Arabia<br/>Transfection<br/>United States