Association of PALB2 sequence variants with the risk of familial and early-onset breast cancer in a South-American population
2015
Background
Germline mutations in PALB2 have been identified in approximately 1% of familial breast cancer (BC) in several populations. Nevertheless its contribution in the South-American population is unknown. The goal of this study was to determine the prevalence of PALB2 mutations in the Chilean population.
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