2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

Reports of unrelated individuals with autism spectrum disorder (ASD) and similar clinical features having overlapping de novo interstitial deletions at 2p15–p16.1 suggest that this region harbors a gene(s) important to the development of autism. We molecularly characterized two such deletions, selec...

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Detalhes bibliográficos
Main Authors: Liu, Xudong, Malenfant, Patrick, Reesor, Chelsea, Lee, Alana, Hudson, Melissa L, Harvard, Chansonette, Qiao, Ying, Persico, Antonio M, Cohen, Ira L, Chudley, Albert E, Forster-Gibson, Cynthia, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Holden, Jeanette JA
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3230356/
https://ncbi.nlm.nih.gov/pubmed/21750575
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.112
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