“…Mutations in VPS13B lead to Cohen syndrome (Kolehmainen et al, 2003); mutations in VPS13C have been identified as a cause of an autosomal-recessive, early-onset and severe form of Parkinson's disease (Lesage et al, 2016; Schormair et al, 2018); and, most recently, mutations in VPS13D have been linked to other movement disorders (Gauthier et al, 2018; Seong et al, 2018). In addition, genomic data have identified VPS13A-D variants in other neurological disorders (Fromer et al, 2014; McCarthy et al, 2014; Meda et al, 2012), in various types of cancer (An et al, 2012; Furukawa et al, 2011; Morisaki et al, 2014; Park et al, 2016b; Yang et al, 2016b) and in diabetes (Grarup et al, 2011; Saxena et al, 2010; Strawbridge et al, 2011; Windholz et al, 2011).…”