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

2016 . 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, J.M. | Challman, T.D. | Hennig, F. | Fischer, U. | Grimme, A. | Suckow, V. | Musante, L. | Nicholi, J. | Shaw, M. | Lodh, S.P. | Niu, Z. | Rosenfeld, J.A. | Stankiewicz, P. | Jentsch, T. J. | Gecz, J. | Field, M. | Kalscheuer, V.M.