Mutations in the VPS35 gene were identified as the cause of an autosomal dominant form of PD (Vilariño-Güell et al. 2011; Zimprich et al. 2011) and mutations in the VPS13C gene were identified as the cause of autosomal recessive form of PD (Lesage et al. 2016). This evidence concerns the gene VPS13C and Parkinson disease.