Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

van der Zee, J; Van Langenhove, T; Kovacs, Gg; Dillen, L; Deschamps, W; Engelborghs, S; Matěj, R; Vandenbulcke, M; Sieben, A; Dermaut, B; Smets, K; Van Damme, P; Merlin, C; Laureys, A; Van Den Broeck, M; Mattheijssens, M; Peeters, K; Benussi, L; Binetti, G; Ghidoni, R; Borroni, Barbara; Padovani, Alessandro; Archetti, S; Pastor, P; Razquin, C; Ortega Cubero, S; Hernández, I; Boada, M; Ruiz, A; de Mendonça, A; Miltenberger Miltényi, G; do Couto, Fs; Sorbi, S; Nacmias, B; Bagnoli, S; Graff, C; Chiang, Hh; Thonberg, H; Perneczky, R; Diehl Schmid, J; Alexopoulos, P; Frisoni, Gb; Bonvicini, C; Synofzik, M; Maetzler, W; vom Hagen, Jm; Schöls, L; Haack, Tb; Strom, Tm; Prokisch, H; Dols Icardo, O; Clarimón, J; Lleó, A; Santana, I; Almeida, Mr; Santiago, B; Heneka, Mt; Jessen, F; Ramirez, A; Sanchez Valle, R; Llado, A; Gelpi, E; Sarafov, S; Tournev, I; Jordanova, A; Parobkova, E; Fabrizi, Gm; Testi, S; Salmon, E; Ströbel, T; Santens, P; Robberecht, W; De Jonghe, P; Martin, Jj; Cras, P; Vandenberghe, R; De Deyn, Pp; Cruts, M; Sleegers, K; Van Broeckhoven, C.