Palmer, E. E., Stuhlmann, T., Weinert, S., Haan, E., van Esch, H., Holvoet, M., Boyle, J., Leffler, M., Raynaud, M., Moraine,
C., van Bokhoven, H., Kleefstra, T., Kahrizi, K., Najmabadi, H., Ropers, H.-H., Delgado, M. R., Sirsi, D., Golla, S., Sommer,
A., Pietryga, M. P., Chung, W. K., Wynn, J., Rohena, L., Bernardo, E., Hamlin, D., Faux, B. M., Grange, D. K., Manwaring,
L., Tolmie, J., Joss, S., Study, D. D. D., Cobben, J. M., Duijkers, F. A. M., Goehringer, M., Challman, T. D., Hennig, F.,
Fischer, U., Grimme, A., Suckow, V., Musante, L., Nicholl, J., Shaw, M., Lodh, S. P., Niu, Z., Rosenfeld, A., Stankiewicz,
P., Jentsch, T. H., Gecz, J., Field, M., & Kalscheuer, V. M. (2018). De novo and
inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure
disorders in males and females. Molecular Psychiatry, 23(2),
222-230. doi:10.1038/mp.2016.135.