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While PD typically occurs as a sporadic disease, 5-10% of cases occur in a familial manner with mutations in at least 20 genes identified to cause monogenic forms of PD [3]
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The in vitro metabolic data established the half-life of AOD9604 in human serum and identified the primary metabolic pathways responsible for its clearance
2020;79(Suppl 1):E856
Liu et al., 2012)
