Moreover, mutations in the LRRK2, VSP35, and CHCHD2 genes have also been described as PD autosomal dominant causes, while mutations in PRKN, PINK1, DJ-1, ATP13A2, FBXO7, and PLA2G6 genes as PD autosomal recessive [24,25]. The gene discussed is FBXO7; the disease is Parkinson disease.