De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
- Rees, E.
- Han, J.
- Morgan, J.
- Carrera, N.
- Escott-Price, V.
- Pocklington, A.J.
- Duffield, M.
- Hall, L.S.
- Legge, S.E.
- Pardiñas, A.F.
- Richards, A.L.
- Roth, J.
- Lezheiko, T.
- Kondratyev, N.
- Kaleda, V.
- Golimbet, V.
- Parellada, M.
- González-Peñas, J.
- Arango, C.
- Alizadeh, B.Z.
- van Amelsvoort, T.
- Bruggeman, R.
- Cahn, W.
- de Haan, L.
- Luykx, J.J.
- Rutten, B.P.F.
- van Os, J.
- van Winkel, R.
- Gawlik, M.
- Kirov, G.
- Walters, J.T.R.
- Holmans, P.
- O’Donovan, M.C.
- Owen, M.J.
- Show all authors +
ISSN: 1546-1726, 1097-6256
Year of publication: 2020
Volume: 23
Issue: 2
Pages: 179-184
Type: Article