De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder | Journal of Medical Genetics

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Cognitive and behavioural genetics

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De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

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Cite this article as:: Babbs C, Lloyd D, Pagnamenta AT, et al

De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

Journal of Medical Genetics 2014;51:737-747.