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Discovery may Lead to Novel Treatment to Slow Progression of Parkinson's Disease

by Traci Bratton

July 20, 2016
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The research team has shown that the most common genetic cause of Parkinson's disease — a mutant LRRK2 kinase enzyme — contributes to the formation of inclusions in neurons, resembling one of the hallmark pathologies seen in Parkinson's disease.

http://www.medindia.net/news/discovery-may-lead-to-novel-treatment-to-slow-progression-of-parkinsons-disease-161876-1.htm

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