التفاصيل البيبلوغرافية
| العنوان: |
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders |
| المؤلفون: |
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 |
| المصدر: |
Nature neuroscience. 19(4):571 |
| مصطلحات موضوعية: |
Medicin och hälsovetenskap |
| URL الوصول: |
http://kipublications.ki.se/Default.aspx?queryparsed=id:133266719 |
| قاعدة البيانات: |
SwePub |
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