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Breast-Cancer Risk in Families with Mutations in PALB2
Author(s) -
Antonis C. Antoniou,
Silvia Casadei,
Tuomas Heikkinen,
Daniel Barrowdale,
Katri Pylkäs,
Jonathan Roberts,
Andrew Lee,
Deepak Subramanian,
Kim De Leeneer,
Florentia Fostira,
Eva Tomiak,
Susan L. Neuhausen,
Zhi L. Teo,
Sofia Khan,
Kristiina Aittomäki,
Jukka S. Moilanen,
Clare Turnbull,
Sheila Seal,
Graham J. Mann,
Anne Kallioniemi,
Geoffrey J. Lindeman,
Saundra S. Buys,
Irene L. Andrulis,
Paolo Radice,
Carlo Tondini,
Siranoush Manoukian,
Amanda E. Toland,
Penelope Miron,
Jeffrey N. Weitzel,
Susan M. Domchek,
Bruce Poppe,
Kathleen Claes,
Drakoulis Yannoukakos,
Patrick Concan,
Jonine L. Bernstein,
Paul A. James,
Douglas F. Easton,
David E. Goldgar,
John L. Hopper,
Nazneen Rahman,
Paolo Peterlongo,
Heli Nevanlinna,
MaryClaire King,
Fergus J. Couch,
Melissa C. Southey,
Robert Winqvist,
William D. Foulkes,
Marc Tischkowitz
Publication year - 2014
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1400382
Subject(s) - breast cancer , palb2 , medicine , oncology , germline mutation , cancer , population , family history , risk factor , mutation , genetics , biology , environmental health , gene
Germline loss-of-function mutations in PALB2 are known to confer a predisposition to breast cancer. However, the lifetime risk of breast cancer that is conferred by such mutations remains unknown.

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