Background Adult-type granulosa cell tumors of the ovary (aGCTs) are rare tumors that represent 2–5% of ovarian malignancies. The prognosis of this tumor is favorable, and it is characterized by slow

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Table S5 from The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors

卵巢颗粒细胞瘤

FOXL2基因

Table S5

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FOXL2 status in recurrent aGCTs.

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