Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes

Identifying genetic cancer risk factors will lead to improved genetic counseling, cancer prevention and cancer care. Analyzing families with a strong history of breast cancer (BC) has been a successful method to identify genes that contribute to the disease. This has led to discoveries of high-risk...

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Detalles Bibliográficos
Autores principales: Helgadottir, Hafdis T., Thutkawkorapin, Jessada, Lagerstedt-Robinson, Kristina, Lindblom, Annika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289997/
https://www.ncbi.nlm.nih.gov/pubmed/34282249
http://dx.doi.org/10.1038/s41598-021-94316-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289997/
https://www.ncbi.nlm.nih.gov/pubmed/34282249
http://dx.doi.org/10.1038/s41598-021-94316-z

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