Out of the six gene mutations responsible for monogenic PD, two are accountable for autosomal dominant (AD) PD forms (SNCA and LRRK2) and the remaining four for autosomal recessive (AR) PD (PARK2, PINK1, DJ-1, and ATP13A2) (Klein and Westenberger, 2012). This evidence concerns the gene ATP13A2 and Parkinson disease.