SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

1. Marini, C.
2. Scheffer, I.E.
3. Nabbout, R.
4. Mei, D.
5. Cox, K.
6. Dibbens, L.M.
7. McMahon, J.M.
8. Iona, X.
9. Carpintero, R.S.
10. Elia, M.
11. Cilio, M.R.
12. Specchio, N.
13. Giordano, L.
14. Striano, P.
15. Gennaro, E.
16. Cross, J.H.
17. Kivity, S.
18. Neufeld, M.Y.
19. Afawi, Z.
20. Andermann, E.
21. Keene, D.
22. Dulac, O.
23. Zara, F.
24. Berkovic, S.F.
25. Guerrini, R.
26. Mulley, J.C.
27. Show all authors +

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DOI: 10.1111/J.1528-1167.2009.02013.X GOOGLE SCHOLAR lock_openOpen access editor

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