A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

Autism is a childhood neuropsychiatric disorder that, despite exhibiting high heritability, has largely eluded efforts to identify specific genetic variants underlying its etiology. We performed a two-stage genetic study in which genome-wide linkage and family-based association mapping was followed...

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Bibliografiset tiedot
Päätekijät: Arking, Dan E., Cutler, David J., Brune, Camille W., Teslovich, Tanya M., West, Kristen, Ikeda, Morna, Rea, Alexis, Guy, Moltu, Lin, Shin, Cook, Edwin H., Chakravarti, Aravinda
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2008
Aiheet:
Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2253968/
https://ncbi.nlm.nih.gov/pubmed/18179894
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2007.09.015
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