Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

© 2018 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)

Bibliographic Details
Main Author: Philtjens, Stéphanie (author)
Other Authors: Van Mossevelde, Sara (author), van der Zee, Julie (author), Wauters, Eline (author), Dillen, Lubina (author), Vandenbulcke, Mathieu (author), Vandenberghe, Rik (author), Ivanoiu, Adrian (author), Sieben, Anne (author), Willems, Christiana (author), Benussi, Luisa (author), Ghidoni, Roberta (author), Binetti, Giuliano (author), Borroni, Barbara (author), Padovani, Alessandro (author), Pastor, Pau (author), Diez-Fairen, Monica (author), Aguilar, Miquel (author), De Mendonça, Alexandre (author), Miltenberger-Miltenyi, Gabriel (author), Hernández, Isabel (author), Boada, Merce (author), Ruiz, Agustín (author), Nacmias, Benedetta (author), Sorbi, Sandro (author), Almeida, Maria Rosário (author), Santana, Isabel (author), Clarimón, Jordi (author), Lleó, Alberto (author), Frisoni, Giovanni B. (author), Sanchez-Valle, Raquel (author), Lladó, Albert (author), Gómez-Tortosa, Estrella (author), Gelpi, Ellen (author), Van den Broeck, Marleen (author), Peeters, Karin (author), Cras, Patrick (author), De Deyn, Peter P. (author), Engelborghs, Sebastiaan (author), Cruts, Marc (author), Van Broeckhoven, Christine (author)
Format: article
Language:eng
Published: 2021
Subjects:
Frontotemporal dementia
Genetic association
Granulin
Rare variants
Sortilin
Online Access:http://hdl.handle.net/10451/50450
Country:Portugal
Oai:oai:repositorio.ul.pt:10451/50450

Internet

http://hdl.handle.net/10451/50450

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