Associated Papers
High-resolution functional mapping of RAD51C by saturation genome editing.
Olvera-León R et al.
Cell, 2024
Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort.
Bouras A et al.
Cancers, 2023
37444530 (PubMed )
Supplement: cancers-15-03420-s001.zip › cancers-2443339-supplementary.pdf
Homologous recombination-deficient mutation cluster in tumor suppressor RAD51C identified by comprehensive analysis of cancer variants.
Prakash R et al.
Proceedings of the National Academy of Sciences of the United States of America, 2022
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