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- Title
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
- Authors
Chen-Plotkin, Alice S; Martinez-Lage, Maria; Sleiman, Patrick M A; Hu, William; Greene, Robert; Wood, Elisabeth McCarty; Bing, Shaoxu; Grossman, Murray; Schellenberg, Gerard D; Hatanpaa, Kimmo J; Weiner, Myron F; White, Charles L, 3rd; Brooks, William S; Halliday, Glenda M; Kril, Jillian J; Gearing, Marla; Beach, Thomas G; Graff-Radford, Neill R; Dickson, Dennis W; Rademakers, Rosa; Boeve, Bradley F; Pickering-Brown, Stuart M; Snowden, Julie; van Swieten, John C; Heutink, Peter; Seelaar, Harro; Murrell, Jill R; Ghetti, Bernardino; Spina, Salvatore; Grafman, Jordan; Kaye, Jeffrey A; Woltjer, Randall L; Mesulam, Marsel; Bigio, Eileen; Lladó, Albert; Miller, Bruce L; Alzualde, Ainhoa; Moreno, Fermin; Rohrer, Jonathan D; Mackenzie, Ian R A; Feldman, Howard H; Hamilton, Ronald L; Cruts, Marc; Engelborghs, Sebastiaan; De Deyn, Peter P; Van Broeckhoven, Christine; Bird, Thomas D; Cairns, Nigel J; Goate, Allison; Frosch, Matthew P; Riederer, Peter F; Bogdanovic, Nenad; Lee, Virginia M Y; Trojanowski, John Q; Van Deerlin, Vivianna M
- Abstract
To assess the relative frequency of unique mutations and their associated characteristics in 97 individuals with mutations in progranulin (GRN), an important cause of frontotemporal lobar degeneration (FTLD).
- Publication
Archives of neurology, 2011, Vol 68, Issue 4, p488
- ISSN
1538-3687
- Publication type
Journal Article
- DOI
10.1001/archneurol.2011.53