Tsai et al. [63] examined the tau tracer 18F-flortaucipir in 11 patients with nonfluent variant primary progressive aphasia (nfvPPA), 10 with corticobasal syndrome (CBS), 10 bvFTD subjects, two with svPPA, and six with FTD-associated pathogenic genetic mutations, microtubule-associated protein tau (MAPT), five with chromosome nine open reading frame 72 (C9ORF72) association, and one associated with progranulin (GRN) mutation. Here, MAPT is linked to frontotemporal dementia.