TARDBP and mild neurocognitive disorder: Mutations in a number of other genes also cause familial ALS; including mutations in autosomal dominant familial MN disease include fALS types 3 [3], 5 [4], 6 or FUS gene [5, 6], 7 [7], 8 [8], 9 or ANG gene [9], 10 or TDP-43 (TARDBP gene) [10–12], 11 or Figure four gene [13], NF-H gene [14], DAO gene [15], X-linked [16], C90RF72 [17–19], alsin [20] and MND with FTD [21].