Human Genome Epidemiology Literature Finder
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Query Trace: Sclerosis and RHEB[original query] |
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Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder. Molecular autism 2013 4 (1): 5. Bahl Samira, Chiang Colby, Beauchamp Roberta L, Neale Benjamin M, Daly Mark J, Gusella James F, Talkowski Michael E, Ramesh Vija |
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