Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

1. Barajas-Martínez, H.
2. Hu, D.
3. Ferrer, T.
4. Onetti, C.G.
5. Wu, Y.
6. Burashnikov, E.
7. Boyle, M.
8. Surman, T.
9. Urrutia, J.
10. Veltmann, C.
11. Schimpf, R.
12. Borggrefe, M.
13. Wolpert, C.
14. Ibrahim, B.B.
15. Sánchez-Chapula, J.A.
16. Winters, S.
17. Haïssaguerre, M.
18. Antzelevitch, C.