Journal
Nature Communications
Publication Date
2018
Volume
9
Inclusive Pages
4619
Document Type
Open Access Publication
DOI
10.1038/s41467-018-06014-6
Rights and Permissions
Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., . . . Study, D. D. D. (2018). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9, 12. doi:10.1038/s41467-018-06014-6 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Recommended Citation
Willing, Marcia and Fiala, Elise, "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language." Nature Communications. 9, 4619. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/7617
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Author Correction_ CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.pdf (444 kB)