Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

Autism is a genetically complex neurodevelopmental syndrome in which language deficits are a core feature. We describe results from two complimentary approaches used to identify risk variants on chromosome 7 that likely contribute to the etiology of autism. A two-stage association study tested 2758...

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Hoofdauteurs: Alarcón, Maricela, Abrahams, Brett S., Stone, Jennifer L., Duvall, Jacqueline A., Perederiy, Julia V., Bomar, Jamee M., Sebat, Jonathan, Wigler, Michael, Martin, Christa L., Ledbetter, David H., Nelson, Stanley F., Cantor, Rita M., Geschwind, Daniel H.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Human Genetics 2008
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2253955/
https://ncbi.nlm.nih.gov/pubmed/18179893
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2007.09.005
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