| Literature DB >> 16455195 |
Sei Hyun Ahn1, Byung Ho Son, Kyung-Sik Yoon, Dong-Young Noh, Wonshik Han, Sung-Won Kim, Eun Sook Lee, Hai-Lin Park, Young Joon Hong, Jae Jin Choi, Seo Yun Moon, Mi Jeong Kim, Kye Hyun Kim, Beom Seok Kwak, Dae-Yeon Cho.
Abstract
We analyzed the mutation spectrum of BRCA1 and BRCA2 genes in 354 Korean breast cancer patients. Overall, 40 patients carried 25 distinct BRCA1/2 mutations including 12 novel mutations. Seven district mutations were found in multiple unrelated patients, with the BRCA2 c.7480C>T mutation detected in eight unrelated patients, accounting for 50% of the mutations detected in BRCA2. The large number (25/40, 62.5%) of recurrent mutations suggests the possibility of developing a simple screening test for these mutations. The frequency of mutations was related to the number and kinds of risk factors, varying from 10.4 to 25% in the five major risk factor groups. The frequency of BRCA mutations in patients with two or more risk factors was markedly higher than that in patients with one risk factor.Entities:
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Year: 2006 PMID: 16455195 DOI: 10.1016/j.canlet.2005.12.031
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679