Liu, Hui <br/><br/>
Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.  [electronic resource] 

 -  Circulation. Cardiovascular genetics  Aug 2010 
 - 374-85 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1942-3268 
<br/><br/><label>Standard No.: </label>10.1161/CIRCGENETICS.109.930867  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>CHO Cells<br/>COS Cells<br/>Cardiac Conduction System Disease<br/>Cells, Cultured<br/>Chlorocebus aethiops<br/>Cricetinae<br/>Cricetulus<br/>Family<br/>Female<br/>Genes, Dominant<br/>Genetic Linkage<br/>Heart Block--genetics<br/>Humans<br/>Male<br/>Mutation--physiology<br/>Pedigree<br/>TRPM Cation Channels--genetics<br/>Transfection