Windheuser, I. C., Becker, J., Cremer, K., Hundertmark, H., Yates, L. M., Mangold, E., Peters, S., Degenhardt, F., Ludwig, K. U., Zink, A. M., Lessel, D., Bierhals, T., Herget, T., Johannsen, J., Denecke, J., Wohlleber, E., Strom, T. M., Wieczorek, D., Bertoli, M., Colombo, R., Hempel, M., & Engels, H. (2020). nine newly identified individuals refine the phenotype associated with MYT1L mutations. American journal of medical genetics, 182(5), 1021–1031. http://access.bl.uk/ark:/81055/vdc_100102674719.0x00002c