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Moreover, these results provide us with a unique opportunity to recognize BRIP1-induced pro-invasive genes that may serve as biomarkers and/or targets to steer the design of appropriate BC targeted therapies. Fifty-two PD participants (13.4%) and 13 (7.4%) controls carried a GBA variation. GBA status had been strongly associated with GCase activity. Among noncarriers, GCase task had been comparable between PD and settings. Among GBA p.E326K providers (PD, n=20; controls, n=5), task had been considerably red

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