SLC11A2 and Parkinson disease: Incidentally, another form of familial PD was identified with a mutation in the gene coding for the Vacuolar Protein Sorting 35, VPS35 (Zavodszky et al., 2014), which is responsible for the correct endosomal recycling and trafficking of DMT1 (Tabuchi et al., 2010), underpinning the derangement of DMT1 in autophagosomal localization as a basal mechanism involved in the disease.