Cite

    Reuter, M. S., Riess, A., Moog, U., Briggs, T. A., Chandler, K. E., Rauch, A., Stampfer, M., Steindl, K., Gläser, D., Joset, P., , , Krumbiegel, M., Rabe, H., Schulte-Mattler, U., Bauer, P., Beck-Wödl, S., Kohlhase, J., Reis, A., & Zweier, C. (2017). fOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics, 54(1), 64–72. http://access.bl.uk/ark:/81055/vdc_100135174967.0x000039