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A primary luminal/HER2 negative breast cancer patient with mismatch repair deficiency
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-activating the...
Autores principales: | Yang, Xue, Smirnov, Artem, Buonomo, Oreste Claudio, Mauriello, Alessandro, Shi, Yufang, Bischof, Julia, Woodsmith, Jonathan, Melino, Gerry, Candi, Eleonora, Bernassola, Francesca |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545677/ https://www.ncbi.nlm.nih.gov/pubmed/37783677 http://dx.doi.org/10.1038/s41420-023-01650-4 |
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