Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

Individuals with autism are more likely to carry rare inherited and de novo copy number variants (CNVs). However, further research is needed to establish which CNVs are causal and the mechanisms by which these CNVs influence autism. We examined genomic DNA of children with autism (N=41) and healthy...

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Detalhes bibliográficos
Main Authors: Nord, Alex S, Roeb, Wendy, Dickel, Diane E, Walsh, Tom, Kusenda, Mary, O'Connor, Kristen Lewis, Malhotra, Dheeraj, McCarthy, Shane E, Stray, Sunday M, Taylor, Susan M, Sebat, Jonathan, King, Bryan, King, Mary-Claire, McClellan, Jon M
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3110052/
https://ncbi.nlm.nih.gov/pubmed/21448237
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.24
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