학술논문
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
Document Type
Artikel
Author
Rees, E; Walters, JTR; Chambert, KD; O'Dushlaine, C; Szatkiewicz, J; Richards, AL; Georgieva, L; Mahoney-Davies, G; Legge, SE; Moran, JL; Genovese, G; Levinson, D; Morris, DW; Cormican, P; Kendler, KS; O'Neill, FA; Riley, B; Gill, M; Corvin, A; Sklar, P; Hultman, C; Pato, C; Pato, M; Sullivan, PF; Gejman, PV; McCarroll, SA; O'Donovan, MC; Owen, MJ; Kirov, G
Source
Human molecular genetics. 23(6):1669-1676
Subject
Language
English
English
English
ISSN
1460-2083