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A nonsynonymous mutation in PLCG2 reduces the risk of Alzhe..:
van der Lee, Sven J
;
Conway, Olivia J
;
Zettergren, Anna
...
info:eu-repo/semantics/altIdentifier/pmid/pmid:31131421. , 2019
Link:
https://pub.dzne.de/record/140840
RT Journal T1
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
UL https://suche.suub.uni-bremen.de/peid=base-ftdznevdb:oai:pub.dzne.de:140840&Exemplar=1&LAN=DE A1 van der Lee, Sven J A1 Conway, Olivia J A1 Zettergren, Anna A1 Christensen, Kaare A1 Ertekin-Taner, Nilüfer A1 Scholz, Sonja W A1 Ramirez, Alfredo A1 Ruiz, Agustín A1 Slagboom, Eline A1 van der Flier, Wiesje M A1 Holstege, Henne A1 Coppola, G A1 Karydas, A. M A1 Andlauer, Till F M A1 Varpetian, A A1 Foroud, T. M A1 Levey, A. I A1 Kukull, W. A A1 Mendez, M. F A1 Ringman, J A1 Chui, H A1 Cotman, C A1 DeCarli, C A1 Miller, B. L A1 Diez-Fairen, Monica A1 Geschwind, D. H A1 Simon Sanchez, Javier A1 Lleó, Alberto A1 Zetterberg, Henrik A1 Nygaard, Marianne A1 Blauwendraat, Cornelis A1 Savage, Jeanne E A1 Mengel-From, Jonas A1 Jansen, Iris A1 Moreno-Grau, Sonia A1 Wagner, Michael A1 Fortea, Juan A1 Keogh, Michael J A1 Blennow, Kaj A1 Skoog, Ingmar A1 Friese, Manuel A A1 Pletnikova, Olga A1 Zulaica, Miren A1 Lage, Carmen A1 Carrasquillo, Minerva M A1 de Rojas, Itziar A1 Riedel-Heller, Steffi A1 Illán-Gala, Ignacio A1 Wei, Wei A1 Jeune, Bernard A1 Orellana, Adelina A1 Then Bergh, Florian A1 Wang, Xue A1 Hulsman, Marc A1 Beker, Nina A1 Kleineidam, Luca A1 Tesi, Niccolo A1 Morris, Christopher M A1 Indakoetxea, Begoña A1 Collij, Lyduine E A1 Scherer, Martin A1 Morenas-Rodríguez, Estrella A1 Ironside, James W A1 van Berckel, Bart N M A1 Alcolea, Daniel A1 Wiendl, Heinz A1 van den Akker, Erik A1 Strickland, Samantha L A1 Pastor, Pau A1 Rodríguez Rodríguez, Eloy A1 DESGESCO A1 EADB A1 IFGC A1 IPDGC A1 RiMod-FTD A1 Bank, Netherlands Brain A1 Boeve, Bradley F A1 Hernández, Isabel A1 Petersen, Ronald C A1 Ferman, Tanis J A1 van Gerpen, Jay A A1 Reinders, Marcel J T A1 Uitti, Ryan J A1 Tárraga, Lluís A1 Maier, Wolfgang A1 Dols-Icardo, Oriol A1 Kawalia, Amit A1 Dalmasso, Maria Carolina A1 van Eijk, Kristel R A1 Boada, Mercè A1 Zettl, Uwe K A1 van Schoor, Natasja M A1 Beekman, Marian A1 Allen, Mariet A1 Masliah, Eliezer A1 de Munain, Adolfo López A1 Pantelyat, Alexander A1 Wszolek, Zbigniew K A1 Ross, Owen A A1 Stringa, Najada A1 Dickson, Dennis W A1 Graff-Radford, Neill R A1 Knopman, David A1 Rademakers, Rosa A1 Lemstra, Afina W A1 Pijnenburg, Yolande A L A1 Scheltens, Philip A1 Gasser, Thomas A1 Chinnery, Patrick F A1 Hemmer, Bernhard A1 Chen, Jason A A1 Huisman, Martijn A A1 Troncoso, Juan A1 Moreno, Fermin A1 Nohr, Ellen A A1 Sørensen, Thorkild I A A1 Heutink, Peter A1 Sánchez-Juan, Pascual A1 Posthuma, Danielle A1 GIFT A1 Clarimón, Jordi PB Springer YR 2019 K1 info:eu-repo/classification/ddc/610 K1 Alleles K1 Alzheimer Disease: genetics K1 Amyotrophic Lateral Sclerosis: genetics K1 Brain: immunology K1 Brain: metabolism K1 Brain: pathology K1 Dementia: genetics K1 Frontotemporal Dementia: genetics K1 Genetic Predisposition to Disease K1 Genome-Wide Association Study K1 Humans K1 Lewy Body Disease: genetics K1 Longevity: genetics K1 Microglia: metabolism K1 Multiple Sclerosis: genetics K1 Mutation K1 Neuroimaging K1 Parkinson Disease: genetics K1 Phospholipase C gamma: genetics K1 Risk JF info:eu-repo/semantics/altIdentifier/pmid/pmid:31131421 LK http://dx.doi.org/https://pub.dzne.de/record/140840 DO https://pub.dzne.de/record/140840 SF ELIB - SuUB Bremen
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