Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

Autor: Manuel Seijo-Martínez, Lutz Frölich, Wolfgang Maier, Eckart Rüther, M. Lennarz, Frank Jessen, Axel Wetter, Cristina Razquin, Mercè Boada, Anja Slotosch, Fermin Moreno, Lluís Tárraga, Alberto Lleó, Elena Lorenzo, Dmitriy Drichel, Maria A. Pastor, Jordi Gascon, Jaume Campdelacreu, Tanja Duenkel, Juan Fortea, Michael Hüll, Marinella Damian, Steffen Wolfsgruber, Isabel Hernández, Stefanie Heilmann, Alfredo Ramirez, Sara Ortega-Cubero, Hojjat Ahmadzadehfar, Begoña Indakoetxea, Jordi Clarimón, Michael T. Heneka, Jens Wiltfang, Ramón Reñé, Holger Jahn, Adolfo López de Munain, Michael Wagner, Pau Pastor, Christian Luckhaus, Klaus Fliessbach, Ana Gorostidi, Raquel Sánchez-Valle, Oliver Peters, Tim Becker, Agustín Ruiz, Mario Riverol, Johannes Kornhuber, Mathias Thelen, Albert Lladó

Publikováno v: Neurobiology of aging 35(11), 2657.e13-2657.e19 (2014). doi:10.1016/j.neurobiolaging.2014.06.018
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Frontotemporal dementia (FTD) is a clinically and genetically heterogeneous disorder. Rare TREM2 variants have been recently identified in families affected by FTD-like phenotype. However, genetic studies of the role of rare TREM2 variants in FTD hav

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a6e80019e37ef11c65804b388b22f0
https://pubmed.ncbi.nlm.nih.gov/25042114