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...

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Detalles Bibliográficos
Autores principales: Yang, Xue, Smirnov, Artem, Buonomo, Oreste Claudio, Mauriello, Alessandro, Shi, Yufang, Bischof, Julia, Woodsmith, Jonathan, Melino, Gerry, Candi, Eleonora, Bernassola, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
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

Internet

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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