Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.

ABSTRACT: Whole exome sequencing identification of putative founder mutations in non-BRCA1/2 breast cancer patients

ORGANISM(S): Homo sapiens

DISEASE(S): normal

SUBMITTER: Javier Gracia 

PROVIDER: E-MTAB-1172 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress