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

Authors

E E Palmer, University of New South Wales
D K Grange, Washington University School of Medicine in St. Louis
L Manwaring, Washington University School of Medicine in St. Louis
et al

Journal

Molecular Psychiatry

Publication Date

8-23-2016

Volume

23

Issue

2

First Page

222

Last Page

230

Document Type

Open Access Publication

DOI

10.1038/mp.2016.135

Rights and Permissions

Palmer, E., Stuhlmann, T., Weinert, S. et al. 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. Mol Psychiatry 23, 222–230 (2018). doi.org/10.1038/mp.2016.135 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/

Recommended Citation

Palmer, E E; Grange, D K; Manwaring, L; and et al, "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. (2016).
https://digitalcommons.wustl.edu/open_access_pubs/11864