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The glucocerebrosidase 1 gene (GBA1), bi‐allelic variants of which cause Gaucher disease (GD), encodes the lysosomal enzyme glucocerebrosidase (GCase) and is a risk factor for Parkinson Disease (PD). GBA1 variants are linked to a reduction in GCase activity in the brain. Variants in Leucine‐Rich Repeat Kinase 2 (LRRK2), such as the gain‐of‐kinase‐function variant G2019S, cause the most common familial...