Clinical implications of germline mutations in breast cancer genes: RECQL
Author:
Funder
European Research Council
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology
Link
http://link.springer.com/content/pdf/10.1007/s10549-018-05096-6.pdf
Reference25 articles.
1. Cybulski C, Carrot-Zhang J, Kluźniak W et al (2015) Germline RECQL mutations are associated with breast cancer susceptibility. Nat Genet 47:643–646. https://doi.org/10.1038/ng.3284
2. Sun J, Wang Y, Xia Y et al (2015) Mutations in RECQL gene are associated with predisposition to breast cancer. PLoS Genet 11:e1005228. https://doi.org/10.1371/journal.pgen.1005228
3. Kwong A, Shin VY, Cheuk IWY et al (2016) Germline RECQL mutations in high risk Chinese breast cancer patients. Breast Cancer Res Treat 157:211–215. https://doi.org/10.1007/s10549-016-3784-1
4. Nguyen-Dumont T, Myszka A, Karpinski P et al (2018) FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine. BMC Med Genet 19:12. https://doi.org/10.1186/s12881-018-0524-x
5. Li N, Rowley SM, Goode DL et al (2018) Mutations in RECQL are not associated with breast cancer risk in an Australian population. Nat Genet 50:1346–1348. https://doi.org/10.1038/s41588-018-0206-9
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