In particular, the heritability of FTD is primarily characterized by autosomal dominant transmission (detected in 10% of familial disease) in three main genes, i.e., MAPT, progranulin, and chromosome 9 open reading frame 72 (C9orf72), with each of them accounting for 5–10% of overall FTD cases [2,27,28]. Here, GRN is linked to frontotemporal dementia.