Tan, Zhi-Ping <br/><br/>
Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.  [electronic resource] 

 -  Scientific reports  Jul 2014 
 - 5616 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2045-2322 
<br/><br/><label>Standard No.: </label>10.1038/srep05616  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Arrhythmias, Cardiac--etiology<br/>Brugada Syndrome<br/>Cardiac Conduction System Disease<br/>Child<br/>Child, Preschool<br/>Codon, Nonsense--genetics<br/>Death, Sudden--etiology<br/>Exome--genetics<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Heart Conduction System--abnormalities<br/>Humans<br/>Male<br/>Middle Aged<br/>NAV1.5 Voltage-Gated Sodium Channel--genetics<br/>Pedigree<br/>Phenotype<br/>Sodium--metabolism