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

Abstract 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 h...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Hafdis T. Helgadottir, Jessada Thutkawkorapin, Kristina Lagerstedt-Robinson, Annika Lindblom
Format: article
Langue:EN
Publié: Nature Portfolio 2021
Sujets:
R
Q
Accès en ligne:https://doaj.org/article/91c5989be8644f0ab7d8dfce646b1eff
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!