Articles tagged "Dardarin mutation (see LRRK2)"

2016 International Congress
Exome sequencing in the Czech patients with early-onset Parkinson’s disease
D. Kemlink, B. Schormair, O. Fiala, D. Zahorakova, P. Martasek, J. Roth, J. Winkelmann, E. Ruzicka (Praha 2, Czech Republic)
Objective: To evaluate prevalence of disease causing mutations and other rare variants in patients with the Early-Onset Parkinson's disease (EOPD). Background: Currently, there are four…