Fig. 3From: Identification of VPS35 p.D620N mutation-related Parkinson’s disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature reviewChromatograms of direct sequencing of the VPS35 genomic sequence. Genetic analysis reveals a single nucleotide change (c.1858G>A, p.D620N) by Sanger sequencing. The mutation identified in this study was located in the indicated positionBack to article page