Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers

The frequency of the APC I1307K mutation and its association with disease pattern was examined in 996 Ashkenazi women consisting of individuals with either sporadic (n = 382) or hereditary (n = 143) breast and/or ovarian cancer; asymptomatic BRCA1/2 mutation carriers (185delAG, 5382insC and 6174delT...

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Dades bibliogràfiques
Autors principals: Gershoni-Baruch, R, Patael, Y, Dagan, Figer, A, Kasinetz, L, Kadouri, E, Sade, R Bruchim Bar, Friedman, E
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2000
Matèries:
Regular Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2363478/
https://ncbi.nlm.nih.gov/pubmed/10901363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.2000.1248
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