De Zio, Roberta <br/><br/>
Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome.  [electronic resource] 

 -  Journal of cellular and molecular medicine  09 2019 
 - 6331-6342 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1582-4934 
<br/><br/><label>Standard No.: </label>10.1111/jcmm.14521  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Cell Line<br/>Cell Membrane--genetics<br/>Child<br/>ERG1 Potassium Channel--genetics<br/>Electrocardiography--methods<br/>Female<br/>HEK293 Cells<br/>Humans<br/>Long QT Syndrome--genetics<br/>Male<br/>Mutation--genetics<br/>Phenotype<br/>Protein Transport--genetics<br/>Young Adult