Muņoz-Esparza, Carmen <br/><br/>
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing.  [electronic resource] 

 -  Revista espanola de cardiologia (English ed.)  Oct 2015 
 - 861-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1885-5857 
<br/><br/><label>Standard No.: </label>10.1016/j.rec.2014.10.022  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Child, Preschool<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>ERG1 Potassium Channel--genetics<br/>Electrocardiography<br/>Female<br/>Genetic Testing<br/>Heart Conduction System--physiopathology<br/>Heterozygote<br/>Humans<br/>Long QT Syndrome--genetics<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Young Adult