Journal
Nature Communications
Publication Date
2019
Volume
10
Issue
1
First Page
4457
Document Type
Open Access Publication
DOI
10.1038/s41467-019-12428-7
Rights and Permissions
Smeland, M. F., McClenaghan, C., Roessler, H. I., Savelberg, S., Hansen, G. Å. M., Hjellnes, H., . . . van Haaften, G. (2019). ABCC9-related intellectual disability myopathy syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9. Nature Communications, 10(1) doi:10.1038/s41467-019-12428-7 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
McClenaghan, Conor; Harter, Theresa; Sala-Rabanal, Monica; Emfinger, Chris H.; Huang, Yan; Singareddy, Soma S.; Nichols, Colin G.; Gunn, Jamie; Wozniak, David F.; Kovacs, Attila; Remedi, Maria S.; and al., et, "ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9." Nature Communications. 10, 1. 4457 (2019).
https://digitalcommons.wustl.edu/open_access_pubs/8281
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