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Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinsons disease
Pathogenic variants in the LRRK2 gene are one of the most commonly identifiable monogenic causes of Parkinsons disease (PD, PARK-LRRK2). This systematic MDSGene literature review comprehensively summarizes published demographic, clinical, and genetic findings related to LRRK2 variants (https://www.m
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