Abstract
Objective: Low-grade serous ovarian carcinoma (LGSOC) commonly carries mutations in the MAP kinase pathway (KRAS, NRAS, BRAF). Penetrance of mutations in this pathway is reported to be approximately 50%. The role of other mutations in the pathogenesis of this disease is poorly understood. Our objective was to evaluate the penetrance of pathogenic mutations outside of this pathway in a racially diverse population.
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