Loss-of-Function Mutations in the Cardiac Calcium Channel Underlie a New Clinical Entity Characterized by ST-Segment Elevation, Short QT Intervals, and Sudden Cardiac Death
Antzelevitch, Charles, Pollevick, Guido D., Cordeiro, Jonathan M., Casis, Oscar, Sanguinetti, Michael C., Aizawa, Yoshiyasu, Guerchicoff, Alejandra, Pfeiffer, Ryan, Oliva, Antonio, Wollnik, Bernd, Gelber, Philip, Bonaros, Elias P., Burashnikov, Elena, Wu, Yuesheng, Sargent, John D., Schickel, Stefan, Oberheiden, Ralf, Bhatia, Atul, Hsu, Li-Fern, Haïssaguerre, Michel, Schimpf, Rainer, Borggrefe, Martin, Wolpert, Christian·2007·Circulation
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- Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome.D. T. Harrell, T. Ashihara, T. Ishikawa, Ichiko Tominaga, A. Mazzanti, Kazuhiro Takahashi, Y. Oginosawa, H. Abe, K. Maemura, N. Sumitomo et al. · 2015 · International Journal of Cardiology
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