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No supportive evidence for TIA1 gene mutations in a Europea..:
Baradaran-Heravi, Yalda
;
Dillen, Lubina
;
Van Damme, Philip
...
info:eu-repo/semantics/altIdentifier/pmid/pmid:29886022. , 2018
Link:
https://pub.dzne.de/record/140105
RT Journal T1
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
UL https://suche.suub.uni-bremen.de/peid=base-ftdznevdb:oai:pub.dzne.de:140105&Exemplar=1&LAN=DE A1 Baradaran-Heravi, Yalda A1 Dillen, Lubina A1 Van Damme, Philip A1 Cras, Patrick A1 Salmon, Eric A1 Synofzik, Matthis A1 Heutink, Peter A1 Wilke, Carlo A1 Simon Sanchez, Javier A1 Rojas-Garcia, Ricard A1 Turon-Sans, Janina A1 Lleó, Alberto A1 Nguyen, Hung Phuoc A1 Illán-Gala, Ignacio A1 Clarimón, Jordi A1 Borroni, Barbara A1 Padovani, Alessandro A1 Pastor, Pau A1 Diez-Fairen, Monica A1 Aguilar, Miquel A1 Gelpi, Ellen A1 Sanchez-Valle, Raquel A1 Borrego-Ecija, Sergi A1 Van Mossevelde, Sara A1 Matej, Radoslav A1 Parobkova, Eva A1 Nacmias, Benedetta A1 Sorbi, Sandro A1 Bagnoli, Silvia A1 de Mendonça, Alexandre A1 Ferreira, Catarina A1 Fraidakis, Matthew J A1 Diehl-Schmid, Janine A1 Alexopoulos, Panagiotis A1 Baets, Jonathan A1 Almeida, Maria Rosário A1 Santana, Isabel A1 Van Broeckhoven, Christine A1 van der Zee, Julie A1 Consortium, BELNEU A1 Consortium, EU EOD A1 Goeman, Johan A1 Nuytten, Dirk A1 Sieben, Anne A1 De Bleecker, Jan L A1 De Jonghe, Peter A1 Santens, Patrick A1 Versijpt, Jan A1 Michotte, Alex A1 Ivanoiu, Adrian A1 Deryck, Olivier A1 Bergmans, Bruno A1 Willems, Christiana A1 De Klippel, Nina A1 Peeters, Dirk A1 Archettim, Silvana A1 Engelborghs, Sebastiaan A1 Bonomi, Elisa A1 Piaceri, Irene A1 Ferrari, Camilla A1 Simões do Couto, Frederico A1 Verdelho, Ana A1 Miltenberger-Miltényi, Gabriel A1 De Deyn, Peter P A1 Vandenbulcke, Mathieu A1 Vandenberghe, Rik PB Elsevier Science YR 2018 K1 info:eu-repo/classification/ddc/610 K1 White People: genetics K1 Amyotrophic Lateral Sclerosis: genetics K1 Cohort Studies K1 European Continental Ancestry Group: genetics K1 Female K1 Frontotemporal Dementia: genetics K1 Gene Frequency K1 Humans K1 Male K1 Mutation K1 Missense K1 T-Cell Intracellular Antigen-1: genetics K1 T-Cell Intracellular Antigen-1 K1 TIA1 protein K1 human JF info:eu-repo/semantics/altIdentifier/pmid/pmid:29886022 LK http://dx.doi.org/https://pub.dzne.de/record/140105 DO https://pub.dzne.de/record/140105 SF ELIB - SuUB Bremen
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