Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder

Den Hoed, J., De Boer, E., Voisin, N., Guex, N., Snijders Blok, L., Chrast, J., The DDD study, Manwaring, L., Willing, M., Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M. and 27 moreDen Hoed, J., De Boer, E., Voisin, N., Guex, N., Snijders Blok, L., Chrast, J., The DDD study, Manwaring, L., Willing, M., Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M., Rosenfeld, J. A., Radtke, K., Preiksaitiene, E., Ranza, E., Depienne, C., Kuechler, A., Mohammed, S., Hamzavi Abedi, Y., Bonagura, V. R., Zuccarelli, B., Horist, B., Krishnamurthy, V., Kattentidt-Mouravieva, A. A., Granger, L., Petersen, A., Jones, K. L., Sinnema, M., Stegmann, A. P. A., Newbury-Ecob, R., Kini, U., Newbury, D. F., Gilissen, C., Brunner, H., Kleefstra, T., Reymond, A., Vissers, L. E. L. M., & Fisher, S. E. (2020). Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder. Talk presented at the 53rd European Human Genetics Conference (ESHG 2020). online. 2020-06-06 - 2020-06-09.
Publication type
Talk
Publication date
2020

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