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. (Q53809565)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
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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 (English)
Arthur A M Wilde
Michael J Ackerman
Carla Spazzolini
Wataru Shimizu
Isabelle Denjoy
Eric Schulze-Bahr
Heikki Swan
Arthur J Moss
Minoru Horie
Paul A Brink