Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis

1. Corrochano, S.
2. Männikkö, R.
3. Joyce, P.I.
4. McGoldrick, P.
5. Wettstein, J.
6. Lassi, G.
7. Rayan, D.L.R.
8. Blanco, G.
9. Quinn, C.
10. Liavas, A.
11. Lionikas, A.
12. Amior, N.
13. Dick, J.
14. Healy, E.G.
15. Stewart, M.
16. Carter, S.
17. Hutchinson, M.
18. Bentley, L.
19. Fratta, P.
20. Cortese, A.
21. Cox, R.
22. Steve, D.
23. Tucci, V.
24. Wackerhage, H.
25. Amato, A.A.
26. Greensmith, L.
27. Koltzenburg, M.
28. Hanna, M.G.
29. Acevedo-Arozena, A.
30. Show all authors +

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DOI: 10.1093/BRAIN/AWU292 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus