LRRK2 and movement disorder: The aim of this study was to screen a multicentre early onset and familial PD cohort from 9 movement disorder centres across Central Europe within the Central European Group on Genetics of Movement Disorders (CEGEMOD) consortium [17] for rare LRRK2 variants using whole exome sequencing (WES) data to access the possible contribution of proposed p.L1795F LRRK2 variant to PD in Central Europe.