학술논문
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
Document Type
Artikel
Author
van der Zee, J; Van Langenhove, T; Kovacs, GG; Dillen, L; Deschamps, W; Engelborghs, S; Matej, 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, B; Padovani, A; Archetti, S; Pastor, P; Razquin, C; Ortega-Cubero, S; Hernandez, I; Boada, M; Ruiz, A; de Mendonca, A; Miltenberger-Miltenyi, 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; Schols, L; Haack, TB; Strom, TM; Prokisch, H; Dols-Icardo, O; Clarimon, J; Lleo, 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; Strobel, T; Santens, P; Robberecht, W; De Jonghe, P; Martin, JJ; Cras, P; Vandenberghe, R; De Deyn, PP; Cruts, M; Sleegers, K; Van Broeckhoven, C
Source
Acta neuropathologica. 128(3):397-410
Subject
Language
English
English
English
ISSN
1432-0533