A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer FAMILIAL CANCER Kwong, A., Ng, E. K., Tang, E. Y., Wong, C. L., Law, F. B., Leung, C. P., Chan, A., Cheung, M. T., To, M. Y., Ma, E. S., West, D. W., Ford, J. M. 2011; 10 (2): 233-237


Germline mutations in the two breast cancer susceptibility genes, BRCA1 and BRCA2 account for a significant portion of hereditary breast/ovarian cancer. De novo mutations such as multiple exon deletion are rarely occurred in BRCA1 and BRCA2. During our mutation screening for BRCA1/2 genes to Chinese women with risk factors for hereditary breast/ovarian cancer, we identified a novel germline mutation, consisting of a deletion from exons 1 to 12 in BRCA1 gene, in a patient diagnosed with early onset triple negative breast cancer with no family history of cancer. None of her parents carried the mutation and molecular analysis showed that this novel de novo germline mutation resulted in down-regulation of BRCA1 gene expression.

View details for DOI 10.1007/s10689-011-9429-y

View details for Web of Science ID 000290937500008

View details for PubMedID 21404118

View details for PubMedCentralID PMC3100488