| Title: |
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes |
| Authors: |
Lionel, A. C.; Tammimies, K.; Vaags, A. K.; Rosenfeld, J. A.; Ahn, J. W.; Merico, D.; Noor, A.; Runke, C. K.; Pillalamarri, V. K.; Carter, M. T.; Gazzellone, M. J.; Thiruvahindrapuram, B.; Fagerberg, C.; Laulund, L. W.; Pellecchia, G.; Lamoureux, S.; Deshpande, C.; Clayton-Smith, J.; White, A. C.; Leather, S.; Trounce, J.; Melanie Bedford, H.; Hatchwell, E.; Eis, P. S.; Yuen, R. K. C.; Walker, S.; Uddin, M.; Geraghty, M. T.; Nikkel, S. M.; Tomiak, E. M.; Fernandez, B. A.; Soreni, N.; Crosbie, J.; Arnold, P. D.; Schachar, R. J.; Roberts, W.; Paterson, A. D.; So, J.; Szatmari, P.; Chrysler, C.; Woodbury-Smith, M.; Brian Lowry, R.; Zwaigenbaum, L.; Mandyam, D.; Wei, J.; MacDonald, J. R.; Howe, J. L.; Nalpathamkalam, T.; Wang, Z.; Tolson, D. |
| Source: |
Human Molecular Genetics ; volume 23, issue 10, page 2752-2768 ; ISSN 0964-6906 1460-2083 |
| Publisher Information: |
Oxford University Press (OUP) |
| Publication Year: |
2013 |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| DOI: |
10.1093/hmg/ddt669 |
| Availability: |
https://doi.org/10.1093/hmg/ddt669; http://academic.oup.com/hmg/article-pdf/23/10/2752/1698409/ddt669.pdf |
| Accession Number: |
edsbas.87BA708C |
| Database: |
BASE |