Abstract:No disease modifying therapy is currently available for Parkinson's disease (PD), the second most common neurodegenerative disease. The long non-motor prodromal phase of PD is a window of opportunity for early detection and intervention. However, we lack the pathophysiological understanding to develop selective biomarkers and interventions. By developing a mutant a-synuclein selective-overexpression mouse model of prodromal PD, we identified a cellautonomous selective Kv4 channelopathy in dorsal motor nucleus … Show more
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