De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

1. Rees, E.
2. Han, J.
3. Morgan, J.
4. Carrera, N.
5. Escott-Price, V.
6. Pocklington, A.J.
7. Duffield, M.
8. Hall, L.S.
9. Legge, S.E.
10. Pardiñas, A.F.
11. Richards, A.L.
12. Roth, J.
13. Lezheiko, T.
14. Kondratyev, N.
15. Kaleda, V.
16. Golimbet, V.
17. Parellada, M.
18. González-Peñas, J.
19. Arango, C.
20. Alizadeh, B.Z.
21. van Amelsvoort, T.
22. Bruggeman, R.
23. Cahn, W.
24. de Haan, L.
25. Luykx, J.J.
26. Rutten, B.P.F.
27. van Os, J.
28. van Winkel, R.
29. Gawlik, M.
30. Kirov, G.
31. Walters, J.T.R.
32. Holmans, P.
33. O’Donovan, M.C.
34. Owen, M.J.
35. Mostrar todos los/as autores/as +