Journal
European Journal of Human Genetics
Publication Date
7-5-2019
Volume
27
Issue
10
First Page
1611
Last Page
1618
Document Type
Open Access Publication
DOI
10.1038/s41431-019-0462-x
Rights and Permissions
Dyment, D.A., Terhal, P.A., Rustad, C.F. et al. De novo substitutions of TRPM3 cause intellectual disability and epilepsy. Eur J Hum Genet 27, 1611–1618 (2019). doi.org/10.1038/s41431-019-0462-x 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
Dyment, David A; Terhal, Paulien A; Rustad, Cecilie F; Tveten, Kristian; Griffith, Christopher; Jayakar, Parul; Shinawi, Marwan; Ellingwood, Sara; Smith, Rosemarie; van Gassen, Koen; McWalter, Kirsty; Innes, A Micheil; and Lines, Matthew A, "De novo substitutions of TRPM3 cause intellectual disability and epilepsy." European Journal of Human Genetics. 27, 10. 1611 - 1618. (2019).
https://digitalcommons.wustl.edu/open_access_pubs/11842
