Parkinsonism is found in approximately 20–30% of patients in FTLD; in particular, it is frequently observed in familial FTD, with mutations linked to microtubule associated protein Tau (MAPT), progranulin (GRN or PGRN), and chromosome 9 open reading frame 72 (C9ORF72) repeat expansion [49]. The gene discussed is GRN; the disease is Parkinsonism.