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

MLA

Babbs, Christian, et al. “De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder.” Journal of Medical Genetics, vol. 51, no. 11, Nov. 2014, pp. 737–47. EBSCOhost, https://doi.org/10.1136/jmedgenet-2014-102582.

APA

Babbs, C., Lloyd, D., Pagnamenta, A. T., Twigg, S. R. F., Green, J., McGowan, S. J., Mirza, G., Naples, R., Sharma, V. P., Volpi, E. V., Buckle, V. J., Wall, S. A., Knight, S. J. L., Parr, J. R., & Wilkie, A. O. M. (2014). De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. Journal of Medical Genetics, 51(11), 737–747. https://doi.org/10.1136/jmedgenet-2014-102582

Chicago

Babbs, Christian, Deborah Lloyd, Alistair T Pagnamenta, Stephen R F Twigg, Joanne Green, Simon J McGowan, Ghazala Mirza, et al. 2014. “De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder.” Journal of Medical Genetics 51 (11): 737–47. doi:10.1136/jmedgenet-2014-102582.