Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

Smith, Bn; Ticozzi, N; Fallini, C; Gkazi, As; Topp, S; Kenna, Kp; Scotter, El; Kost, J; Keagle, P; Miller, Jw; Calini, D; Vance, C; Danielson, Ew; Troakes, C; Tiloca, C; Al Sarraj, S; Lewis, Ea; King, A; Colombrita, C; Pensato, V; Castellotti, B; de Belleroche, J; Baas, F; ten Asbroek, Al; Sapp, Pc; McKenna Yasek, D; Mclaughlin, Rl; Polak, M; Asress, S; Esteban Pérez, J; Muñoz Blanco, Jl; Simpson, M; Slagen, Consortium; van Rheenen, W; Diekstra, Fp; Lauria, G; Duga, S; Corti, S; Cereda, C; Corrado, L; Sorarù, G; Morrison, Ke; Williams, Kl; Nicholson, Ga; Blair, Ip; Dion, Pa; Leblond, Cs; Rouleau, Ga; Hardiman, O; Veldink, Jh; van den Berg, Lh; Al Chalabi, A; Pall, H; Shaw, Pj; Turner, Mr; Talbot, K; Taroni, F; García Redondo, A; Wu, Z; Glass, Jd; Gellera, C; Ratti, A; Brown RH, Jr; Silani, V; Comi, Giancarlo; Shaw, Ce; Landers, Je