Rare Mutations in RINT1 Predispose Carriers to Breast and Lynch Syndrome-Spectrum Cancers
- Author(s):
- Park, D.J.; Tao, K.; Calvez-Kelm, F. le; Tu, N.D.; Robinot, N.; Hammet, F.; Odefrey, F.; Tsimiklis, H.; Teo, Z.L.; Thingholm, L.B.; Young, E.L.; Voegele, C.; Lonie, A.; Pope, B.J.; Roane, T.C.; Bell, R.; Hu, H.; Shankaracharya; Huff, C.D.; Ellis, J.; Li, J.; Makunin, I.V.; John, E.M.; Andrulis, I.L.; Terry, M.B.; Daly, M.; Buys, S.S.; Snyder, C.; Lynch, H.T.; Devilee, P. (0000-0002-8023-2009); Giles, G.G.; Hopper, J.L.; Feng, B.J.; Lesueur, F.; Tavtigian, S.V.; Southey, M.C.; Goldgar, D.E.
- Published
- 2014
- Publication type
- Article / Letter to editor
- Date issued
- 2014-07-31
- Language
- English
- Is part of
- Cancer Discovery (2014), Vol. 4, no. 7, p. 804-815
- hdl
- 1887/107726
- doi
- 10.1158/2159-8290.CD-14-0212