Crotti, Lia <br/><br/>
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.  [electronic resource] 

 -  Circulation  Nov 2007 
 - 2366-75 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1524-4539 
<br/><br/><label>Standard No.: </label>10.1161/CIRCULATIONAHA.107.726950  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Ethnicity--genetics<br/>Female<br/>Humans<br/>International Cooperation<br/>KCNQ1 Potassium Channel--genetics<br/>Long QT Syndrome--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Risk Factors<br/>Severity of Illness Index