Journal
Breast cancer research
Publication Date
10-2-2023
Volume
25
Issue
1
First Page
112
Document Type
Open Access Publication
DOI
10.1186/s13058-023-01718-0
Rights and Permissions
Gerratana, L., Davis, A.A., Velimirovic, M. et al. Interplay between ESR1/PIK3CA codon variants, oncogenic pathway alterations and clinical phenotype in patients with metastatic breast cancer (MBC): comprehensive circulating tumor DNA (ctDNA) analysis. Breast Cancer Res 25, 112 (2023). https://doi.org/10.1186/s13058-023-01718-0 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Recommended Citation
Gerratana, Lorenzo; Davis, Andrew A; Clifton, Katherine; Hensing, Whitney L; Ma, Cynthia X; and et al., "Interplay between ESR1/PIK3CA codon variants, oncogenic pathway alterations and clinical phenotype in patients with metastatic breast cancer (MBC): Comprehensive circulating tumor DNA (ctDNA) analysis." Breast cancer research. 25, 1. 112 (2023).
https://digitalcommons.wustl.edu/oa_4/2482
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
