What is it about?
There are many gene variants which have no effect, or whose effect we don't understand in breast cancer. This paper helps to categorize variants that affect gene expression.
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Why is it important?
The majority of individuals at risk for breast cancer do not have an obvious mutation that is responsible for their risk. This study attempts to find these mutations.
Read the Original
This page is a summary of: Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predisposition, Breast Cancer Research and Treatment, December 2017, Springer Science + Business Media,
DOI: 10.1007/s10549-017-4602-0.
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