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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Por Coppola, Giovanni, Chinnathambi, Subashchandrabose, Lee, Jason JiYong, Dombroski, Beth A., Baker, Matt C., Soto-Ortolaza, Alexandra I., Lee, Suzee E., Klein, Eric, Huang, Alden Y., Sears, Renee, Lane, Jessica R., Karydas, Anna M., Kenet, Robert O., Biernat, Jacek, Wang, Li-San, Cotman, Carl W., DeCarli, Charles S., Levey, Allan I., Ringman, John M., Mendez, Mario F., Chui, Helena C., Le Ber, Isabelle, Brice, Alexis, Lupton, Michelle K., Preza, Elisavet, Lovestone, Simon, Powell, John, Graff-Radford, Neill, Petersen, Ronald C., Boeve, Bradley F., Lippa, Carol F., Bigio, Eileen H., Mackenzie, Ian, Finger, Elizabeth, Kertesz, Andrew, Caselli, Richard J., Gearing, Marla, Juncos, Jorge L., Ghetti, Bernardino, Spina, Salvatore, Bordelon, Yvette M., Tourtellotte, Wallace W., Frosch, Matthew P., Vonsattel, Jean Paul G., Zarow, Chris, Beach, Thomas G., Albin, Roger L., Lieberman, Andrew P., Lee, Virginia M., Trojanowski, John Q., Van Deerlin, Vivianna M., Bird, Thomas D., Galasko, Douglas R., Masliah, Eliezer, White, Charles L., Troncoso, Juan C., Hannequin, Didier, Boxer, Adam L., Geschwind, Michael D., Kumar, Satish, Mandelkow, Eva-Maria, Wszolek, Zbigniew K., Uitti, Ryan J., Dickson, Dennis W., Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Ross, Owen A., Rademakers, Rosa, Schellenberg, Gerard D., Miller, Bruce L., Mandelkow, Eckhard, Geschwind, Daniel H.
Publicado em 2012
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