Journal
Scientific Reports
Publication Date
10-8-2021
Volume
11
Issue
1
First Page
19999
Document Type
Open Access Publication
DOI
10.1038/s41598-021-99278-w
Rights and Permissions
McNulty, S.N., Schwetye, K.E., Ferguson, C. et al. BRAF mutations may identify a clinically distinct subset of glioblastoma. Sci Rep 2021 Oct 8; 11(1): 19999. DOI: 10.1038/s41598-021-99278-w. https://www.nature.com/articles/s41598-021-99278-w 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
Recommended Citation
McNulty, Samantha N; Schwetye, Katherine E; Ferguson, Cole; Storer, Chad E; Ansstas, George; Kim, Albert H; Gutmann, David H; Rubin, Joshua B; Head, Richard D; and Dahiya, Sonika, "BRAF mutations may identify a clinically distinct subset of glioblastoma." Scientific Reports. 11, 1. 19999 (2021).
https://digitalcommons.wustl.edu/open_access_pubs/11065
Supplementary Figure 1
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Supplementary Figure 3
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Supplementary Figure 4
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Supplementary Legends
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Supplementary Table 1
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Supplementary Table 2
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Supplementary Table 3
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Supplementary Table 4
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Supplementary Table 5
