GBA1 mutations increase α-synuclein aggregation risk through glucosylceramide accumulation. Enhancement of GCase activity via chaperone therapy (ambroxol) or substrate reduction (GCS inhibitors) represents the strongest therapeutic approach with active clinical trials, favorable safety profile, and FDA orphan designation for genetically-defined PD subtype.
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No DepMap CRISPR Chronos data found for GBA1.
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