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Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers.
Cancer Discov. 2014 Jul;4(7):804-15. doi: 10.1158/2159-8290.CD-14-0212. Epub 2014 May 2.
Cancer Discov. 2014.
PMID: 25050558
Free PMC article.
Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study.
Damiola F, Pertesi M, Oliver J, Le Calvez-Kelm F, Voegele C, Young EL, Robinot N, Forey N, Durand G, Vallée MP, Tao K, Roane TC, Williams GJ, Hopper JL, Southey MC, Andrulis IL, John EM, Goldgar DE, Lesueur F, Tavtigian SV.
Damiola F, et al. Among authors: roane tc.
Breast Cancer Res. 2014 Jun 3;16(3):R58. doi: 10.1186/bcr3669.
Breast Cancer Res. 2014.
PMID: 24894818
Free PMC article.
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