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.

2014-01-01