A primary luminal/HER2 negative breast cancer patient with mismatch repair deficiency
Abstract Here, we present the case of a 47-year-old woman diagnosed with luminal B breast cancer subtype and provide an in-depth analysis of her gene mutations, chromosomal alterations, mRNA and protein expression changes. We found a point mutation in the FGFR2 gene, which is potentially hyper-activ...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2023-10-01
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Series: | Cell Death Discovery |
Online Access: | https://doi.org/10.1038/s41420-023-01650-4 |