Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
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author: Dennis W. Dickson, Alexis Brice, Margaret A. Pericak-Vance, Eva-Maria Mandelkow, Renee L. Sears, Elizabeth Finger, Simon Lovestone, Lindsay A. Farrer, Eckhard Mandelkow, Charles L White, John Q. Trojanowski, Elisavet Preza, Richard Mayeux, Ryan J Uitti, Zbigniew K Wszolek, Eliezer Masliah, Rosa Rademakers, Ronald C. Petersen, Bruce L. Miller, Owen A. Ross, Michelle K Lupton, Jonathan L Haines, Thomas G Beach, Didier Hannequin, Adam L Boxer, Daniel Geschwind, Bradley F Boeve, Bernardino F. Ghetti, Matthew Frosch, Michael Geschwind, Neill R Graff-Radford, Suzee E Lee, Robert A. Stern, Matt Baker, Anna M Karydas, Giovanni Coppola, Carol F Lippa, Eileen H Bigio, Vivianna M Van Deerlin, Isabelle Le Ber, Alexandra I Soto-Ortolaza, Douglas R. Galasko, Marla Gearing, Jean Paul G Vonsattel, Juan C Troncoso, Yvette Bordelon, Mario F Mendez, Beth A Dombroski, Roger L Albin, Helena Chui, Allan Levey, Andrew P Lieberman, John M Ringman, Alzheimer's Disease Genetics Consortium, Gerard D Schellenberg, Charles DeCarli, Jorge L Juncos, Alden Y Huang, Ian R Mackenzie, Carl Cotman
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