학술논문
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Document Type
Artikel
Author
Singh, T; Kurki, MI; Curtis, D; Purcell, SM; Crooks, L; Mcrae, J; Suvisaari, J; Chheda, H; Blackwood, D; Breen, G; Pietilainen, O; Gerety, SS; Ayub, M; Blyth, M; Cole, T; Collier, D; Coomber, EL; Craddock, N; Daly, MJ; Danesh, J; DiForti, M; Foster, A; Freimer, NB; Geschwind, D; Johnstone, M; Joss, S; Kirov, G; Korkko, J; Kuismin, O; Holmans, P; Hultman, CM; Iyegbe, C; Lonnqvist, J; Mannikko, M; McCarroll, SA; McGuffin, P; McIntosh, AM; McQuillin, A; Moilanen, JS; Moore, C; Murray, RM; Newbury-Ecob, R; Ouwehand, W; Paunio, T; Prigmore, E; Rees, E; Roberts, D; Sambrook, J; Sklar, P; St Clair, D; Veijola, J; Walters, JTR; Williams, H; Sullivan, PF; Hurles, ME; O'Donovan, MC; Palotie, A; Owen, MJ; Barrett, JC
Source
Nature neuroscience. 19(4):571
Subject
Language
English
English
English
ISSN
1546-1726