Prevalence of BRCA1 and BRCA2 mutations in non-familial breast cancer patients with high risks in Korea: The Korean Hereditary Breast Cancer (KOHBRA) Study

@inproceedings{Son2012PrevalenceOB,
  title={Prevalence of BRCA1 and BRCA2 mutations in non-familial breast cancer patients with high risks in Korea: The Korean Hereditary Breast Cancer (KOHBRA) Study},
  author={Byung Ho Son and Sei Hyun Ahn and Sung-won Kim and Eunyoung Kang and Sue Kyung Park and Min Hyuk Lee and Woo-Chul Noh and Lee Su Kim and Yongsik Jung and Ku Sang Kim and Dong Young Noh and Byung-In Moon and Young Jin Suh and Jeong Eon Lee and Doo Ho Choi and Sung Yong Kim and Sung Hoo Jung and Cha Kyong Yom and Hyde Lee and J H Yang},
  booktitle={Breast Cancer Research and Treatment},
  year={2012}
}
Prevalence and phenotype of BRCA mutation can vary by race. The purpose of this study is to evaluate the prevalence of BRCA1/2 mutations in non-familial breast cancer patients with high risks in Korea. A subset of 758 patients was selected for this study from the KOHBRA nationwide multicenter prospective cohort study. Mutations in BRCA1/2 genes were tested using fluorescent-conformation sensitive gel electrophoresis, denaturing high performance liquid chromatography or direct sequencing… CONTINUE READING
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