Germline BRCA1/2 Variants in Polish Patients with Family History of Breast and Ovarian Cancer: Prevalence, CNV Detection, and Identification of a Novel Loss-of-Function Mutation
These results emphasize the difficulties involved in molecular diagnostics and indicate the need for further research into new predictive models for patients with hereditary breast and ovarian cancer.
Authors
- Izabela Dróźdż (ORCID: https://orcid.org/0000-0003-1956-5063)
- Hanna Moczulska (ORCID: https://orcid.org/0000-0002-1815-3326)
- Karolina Zezawska
- Olga Wojtyczka (ORCID: https://orcid.org/0000-0003-4754-7524)
- Agnieszka Zmysłowska (ORCID: https://orcid.org/0000-0001-8781-4469)
- Katarzyna Piekarska (ORCID: https://orcid.org/0000-0002-6975-5298)
- Marcin Serafin
- Sebastian Skoczylas (ORCID: https://orcid.org/0000-0003-2760-2397)
- Tomasz Płoszaj
Institutions
- Medical University of Lodz (PL)
Publication Details
- Journal
- Current Oncology
- Published
- 2025-12-24
- DOI
- https://doi.org/10.3390/curroncol33010010
- Primary Topic
- BRCA gene mutations in cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00