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Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). [electronic resource] by
- Templin, Christian
- Ghadri, Jelena-Rima
- Rougier, Jean-Sébastien
- Baumer, Alessandra
- Kaplan, Vladimir
- Albesa, Maxime
- Sticht, Heinrich
- Rauch, Anita
- Puleo, Colleen
- Hu, Dan
- Barajas-Martinez, Héctor
- Antzelevitch, Charles
- Lüscher, Thomas F
- Abriel, Hugues
- Duru, Firat
Producer: 20120105
In:
European heart journal vol. 32
Availability: No items available.
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