Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.
Autor: | Bahl, Samira1, Chiang, Colby1, Beauchamp, Roberta L.1, Neale, Benjamin M.1,2,3, Daly, Mark J.1,2,3, Gusella, James F.1,3,4, Talkowski, Michael E.1,3, Ramesh, Vijaya1 ramesh@helix.mgh.harvard.edu |
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Zdroj: | Molecular Autism. 2013, Vol. 4 Issue 1, p1-11. 11p. 1 Diagram, 4 Charts, 1 Graph. |
Databáze: | Academic Search Ultimate |
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