While the majority of ALS cases are considered sporadic, most cases of familial ALS arise from genetic mutations in the genes encoding superoxide dismutase 1 (SOD1), Alsin (ALS2), TDP-43, chromosome 9 open reading frame 72 (C9ORF72), and fused in sarcoma (FUS) [227]. The gene discussed is TARDBP; the disease is amyotrophic lateral sclerosis.