RT @ScienceofPD: An analysis of the prevalence of LRRK2, SNCA, & VPS35 mutations & associated clinical features in a large French multi-cen…
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An analysis of the prevalence of LRRK2, SNCA, & VPS35 mutations & associated clinical features in a large French multi-center cohort of #Parkinsons (n=1,805) https://t.co/XdxNBRXgJX https://t.co/jdJ22Qva1m
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New Research: Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort: LRRK2, SNCA, and VPS35 are unequivocally associated with autosomal dominant Parkinson's disease (PD). We evaluated the… https://t.co/R5x66L