학술논문
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Document Type
Artikel
Author
Lionel, AC; Tammimies, K; Vaags, AK; Rosenfeld, JA; Ahn, JW; Merico, D; Noor, A; Runke, CK; Pillalamarri, VK; Carter, MT; Gazzellone, MJ; Thiruvahindrapuram, B; Fagerberg, C; Laulund, LW; Pellecchia, G; Lamoureux, S; Deshpande, C; Clayton-Smith, J; White, AC; Leather, S; Trounce, J; Bedford, HM; Hatchwell, E; Eis, PS; Yuen, RKC; Walker, S; Uddin, M; Geraghty, MT; Nikkel, SM; Tomiak, EM; Fernandez, BA; Soreni, N; Crosbie, J; Arnold, PD; Schachar, RJ; Roberts, W; Paterson, AD; So, J; Szatmari, P; Chrysler, C; Woodbury-Smith, M; Lowry, RB; Zwaigenbaum, L; Mandyam, D; Wei, J; MacDonald, JR; Howe, JL; Nalpathamkalam, T; Wang, ZZ; Tolson, D; Cobb, DS; Wilks, TM; Sorensen, MJ; Bader, PI; An, Y; Wu, BL; Musumeci, SA; Romano, C; Postorivo, D; Nardone, AM; Della Monica, M; Scarano, G; Zoccante, L; Novara, F; Zuffardi, O; Ciccone, R; Antona, V; Carella, M; Zelante, L; Cavalli, P; Poggiani, C; Cavallari, U; Argiropoulos, B; Chernos, J; Brasch-Andersen, C; Speevak, M; Fichera, M; Ogilvie, CM; Shen, YP; Hodge, JC; Talkowski, ME; Stavropoulos, DJ; Marshall, CR; Scherer, SW
Source
Human molecular genetics. 23(10):2752-2768
Subject
Language
English
English
English
ISSN
1460-2083