BRCA1/2 Mutation Detection in the Tumor Tissue from Selected Polish Patients with Breast Cancer Using Next Generation Sequencing

(1) Background: Although, in the mutated BRCA detected in the Polish population of patients with breast cancer, there is a large percentage of recurrent pathogenic variants, an increasing need for the assessment of rare BRCA1/2 variants using NGS can be observed. (2) Methods: We studied 75 selected...

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Detalles Bibliográficos
Autores principales: Szczerba, Ewelina, Kamińska, Katarzyna, Mierzwa, Tomasz, Misiek, Marcin, Kowalewski, Janusz, Lewandowska, Marzena Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065856/
https://www.ncbi.nlm.nih.gov/pubmed/33918338
http://dx.doi.org/10.3390/genes12040519

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065856/
https://www.ncbi.nlm.nih.gov/pubmed/33918338
http://dx.doi.org/10.3390/genes12040519

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