Mutations in SCN10A are responsible for a large fraction of cases of brugada syndrome
Gespeichert in:
| Hauptverfasser: | , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2014
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| In: |
Journal of the American College of Cardiology
Year: 2014, Jahrgang: 64, Heft: 1, Pages: 66-79 |
| ISSN: | 1558-3597 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: http://www.sciencedirect.com/science/article/pii/S0735109714023584
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| Verfasserangaben: | Hu, Dan; Barajas-Martinez, Hector; Pfeiffer, Ryan; Dezi, Fabio; Pfeiffer, Jenna; Buch, Tapan; Betzenhauser, Matthew J.; Belardinelli, Luiz; Kahlig, Kristopher M.; Rajamani, Sridharan; DeAntonio, Harry J.; Myerburg, Robert J.; Ito, Hiroyuki; Deshmukh, Pramod; Marieb, Mark; Nam, Gi-Byoung; Bhatia, Atul; Hasdemir, Can; Haissaguerre, Michel; Veltmann, Christian; Schimpf, Rainer; Borggrefe, Martin; Viskin, Sami; Antzelevitch, Charles |
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