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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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Enregistré dans:
Détails bibliographiques
Publié dans:Sci Rep
Auteurs principaux: Helgadottir, Hafdis T., Thutkawkorapin, Jessada, Lagerstedt-Robinson, Kristina, Lindblom, Annika
Format: Artigo
Langue:Inglês
Publié: Nature Publishing Group UK 2021
Sujets:
Accès en ligne: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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