Hamdani, N., Akın, I., & El-Battrawy, I. (2026). Gene-therapy in inherited channelopathies like short-QT syndrome: A robust direction towards precision medicine. European heart journal, 47(2), . https://doi.org/10.1093/eurheartj/ehaf831
Chicago-Zitierstil (17. Ausg.)Hamdani, Nazha, Ibrahim Akın, und Ibrahim El-Battrawy. "Gene-therapy in Inherited Channelopathies like Short-QT Syndrome: A Robust Direction Towards Precision Medicine." European Heart Journal 47, no. 2 (2026). https://doi.org/10.1093/eurheartj/ehaf831.
MLA-Zitierstil (9. Ausg.)Hamdani, Nazha, et al. "Gene-therapy in Inherited Channelopathies like Short-QT Syndrome: A Robust Direction Towards Precision Medicine." European Heart Journal, vol. 47, no. 2, 2026, https://doi.org/10.1093/eurheartj/ehaf831.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.