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/)

Detalhes bibliográficos
Autor principal: Philtjens, Stéphanie (author)
Outros Autores: 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)
Formato: article
Idioma:eng
Publicado em: 2021
Assuntos:
Frontotemporal dementia
Genetic association
Granulin
Rare variants
Sortilin
Texto completo:http://hdl.handle.net/10451/50450
País:Portugal
Oai:oai:repositorio.ul.pt:10451/50450
Descrição
Resumo:© 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/)

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