Kuechler, A., Zink, A., Wieland, T., Lüdecke, H., Cremer, K., Salviati, L.,https://doi.org/10.1038/ejhg.2014.165__Engels, H. (2015). Loss-of-function variants of SET cause intellectual disability and the core phenotype of microdeletion 3.3 syndrome. European Journal of Human Genetics. Nature Publishing Group.https://doi.org/10.1038/ejhg.2014.165 

Novarino, G., Fenstermaker, A., Zaki, M., Hofree, M., Silhavy, J., Heiberg, A.,https://doi.org/10.1126/science.1247363__Gleeson, J. (2014). Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science. American Association for the Advancement of Science.https://doi.org/10.1126/science.1247363