학술논문
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative
Document Type
Article
Author
Rademakers, Rosa; Baker, Matt; Gass, Jennifer; Adamson, Jennifer; Huey, Edward D; Momeni, Parastoo; Spina, Salvatore; Coppola, Giovanni; Karydas, Anna M; Stewart, Heather; Johnson, Nancy; Hsiung, Ging-Yuek; Kelley, Brendan; Kuntz, Karen; Steinbart, Ellen; Wood, Elisabeth McCarty; Yu, Chang-En; Josephs, Keith; Sorenson, Eric; Womack, Kyle B; Weintraub, Sandra; Pickering-Brown, Stuart M; Schofield, Peter R; Brooks, William S; Van Deerlin, Vivianna M; Snowden, Julie; Clark, Christopher M; Kertesz, Andrew; Boylan, Kevin; Ghetti, Bernardino; Neary, David; Schellenberg, Gerard D; Beach, Thomas G; Mesulam, Marsel; Mann, David; Grafman, Jordan; Mackenzie, Ian R; Feldman, Howard; Bird, Thomas; Petersen, Ron; Knopman, David; Boeve, Bradley; Geschwind, Dan H; Miller, Bruce; Wszolek, Zbigniew; Lippa, Carol; Bigio, Eileen H; Dickson, Dennis; Graff-Radford, Neill; Hutton, Mike
Source
In Lancet Neurology 2007 6(10):857-868
Subject
Language
ISSN
1474-4422