Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
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author: Christine Van Broeckhoven, Julie van der Zee, Janine Diehl-Schmid, Gabriel Miltenberger-Miltényi, Kristel Sleegers, Radoslav Matěj, Ludger Schöls, Matthis Synofzik, Jennifer Müller Vom Hagen, Sebastiaan Engelborghs, Silvia Testi, Frederico Simões do Couto, Cristina Razquin, Maria R Almeida, Philip Van Damme, Caroline Graff, Alfredo Ramirez, Isabel Santana, Jordi Clarimón, Luisa Benussi, Roberta Ghidoni, Robert Perneczky, Holger Prokisch, Raquel Sanchez-Valle, Rik Vandenberghe, Pau Pastor, Eric Salmon, Benedetta Nacmias, Gabor G. Kovacs, Sandro Sorbi, Giovanni B. Frisoni, Walter Maetzler, Barbara Borroni, Bart Dermaut, Alessandro Padovani, Alexandre de Mendonça, Håkan Thonberg, Ellen Gelpi, Albena Jordanova, Patrick Santens, Wim Robberecht, Peter De Jonghe, Mathieu Vandenbulcke, Lubina Dillen, Alberto Lleó, Stayko Sarafov, Ivailo Tournev, Michael T Heneka, Patrick Cras, Marc Cruts, Katrien Smets, Sara Ortega-Cubero, Giuliano Binetti, Mercè Boada, Silvia Bagnoli, Albert Llado Plarrumani, Gian Maria Fabrizi, Tim Van Langenhove, Anne Sieben, Silvana Archetti, Huei-Hsin Chiang, Beatriz Santiago González, Eva Parobkova, Jean-Jacques Martin, Peter Paul De Deyn, Maria Mattheijssens, Céline Merlin, Marleen Van den Broeck, Oriol Dols Icardo, Tim M Strom, Frank Jessen, Panagiotis Alexopoulos
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