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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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Helgadottir, Hafdis T., Thutkawkorapin, Jessada, Lagerstedt-Robinson, Kristina, Lindblom, Annika
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8289997/
https://ncbi.nlm.nih.gov/pubmed/34282249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-94316-z
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