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). The gene discussed is VPS35; the disease is Parkinson disease.