Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

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