학술논문
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
Document Type
Article
Author
Palmer, E.E.; Boyle, J.; Leffler, M.; Field, M.; Lodh, S.P.; Stuhlmann, T.; Weinert, S.; Jentsch, T.J.; Haan, E.; Shaw, M.; Gecz, J.; Van Esch, H.; Holvoet, M.; Raynaud, M.; Moraine, C.; Van Bokhoven, H.; Kleefstra, T.; Kahrizi, K.; Najmabadi, H.; Ropers, H.-H.; Musante, L.; Kalscheuer, V.M.; 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.; Nicholl, J.; Niu, Z.; Rosenfeld, J.A.; Stankiewicz, P.
Source
In: Molecular Psychiatry . (Molecular Psychiatry, 1 February 2018, 23(2):222-230)
Subject
Language
English
ISSN
14765578
13594184
13594184