Bellin, Milena <br/><br/>
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome.  [electronic resource] 

 -  The EMBO journal  Dec 2013 
 - 3161-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2075 
<br/><br/><label>Standard No.: </label>10.1038/emboj.2013.240  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials--genetics<br/>Adult<br/>Cells, Cultured<br/>ERG1 Potassium Channel<br/>Embryonic Stem Cells--physiology<br/>Ether-A-Go-Go Potassium Channels--genetics<br/>Female<br/>Homeobox Protein Nkx-2.5<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Induced Pluripotent Stem Cells<br/>Long QT Syndrome--genetics<br/>Mutation<br/>Myocytes, Cardiac--pathology<br/>Patch-Clamp Techniques<br/>Phenotype<br/>Pluripotent Stem Cells--physiology<br/>Protein Transport--genetics<br/>Transcription Factors--genetics