![](/img/cover-not-exists.png)
Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)
Templin, C., Ghadri, J.-R., Rougier, J.-S., Baumer, A., Kaplan, V., Albesa, M., Sticht, H., Rauch, A., Puleo, C., Hu, D., Barajas-Martinez, H., Antzelevitch, C., Luscher, T. F., Abriel, H., Duru, F.Volume:
32
Language:
english
Journal:
European Heart Journal
DOI:
10.1093/eurheartj/ehr076
Date:
May, 2011
File:
PDF, 664 KB
english, 2011