High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

Autism spectrum disorders are a group of highly heritable neurodevelopmental disorders with a complex genetic etiology. The International Molecular Genetic Study of Autism Consortium previously identified linkage loci on chromosomes 7 and 2, termed AUTS1 and AUTS5, respectively. In this study, we pe...

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Hlavní autoři: Maestrini, E, Pagnamenta, A T, Lamb, J A, Bacchelli, E, Sykes, N H, Sousa, I, Toma, C, Barnby, G, Butler, H, Winchester, L, Scerri, T S, Minopoli, F, Reichert, J, Cai, G, Buxbaum, J D, Korvatska, O, Schellenberg, G D, Dawson, G, Bildt, A de, Minderaa, R B, Mulder, E J, Morris, A P, Bailey, A J, Monaco, A P
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2010
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2934739/
https://ncbi.nlm.nih.gov/pubmed/19401682
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2009.34
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