Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

著者: Rosa Rademakers, Matt Baker, Jennifer Gass, Jennifer Adamson, Edward D. Huey, Parastoo Momeni, Salvatore Spina, Giovanni Coppola, Anna M. Karydas, Heather Stewart, Nancy Johnson, Ging‐Yuek Robin Hsiung, Brendan Kelley, Karen M. Kuntz, Ellen J. Steinbart, Elisabeth McCarty Wood, Chang-En Yu, Keith A. Josephs, Eric J. Sorenson, Kyle Womack, Sandra Weıntraub, Stuart Pickering‐Brown, Peter R. Schofield, William S. Brooks, Vivianna M. Van Deerlin, Julie S. Snowden, Christopher M. Clark, Andrew Kertesz, Khrista Boylan, Bernardino Ghetti, David Neary, Gerard D Schellenberg, Thomas G. Beach, Marsel Mesulam, David Mann, Jordan Grafman, Ian R. Mackenzie, Howard Feldman, Thomas D. Bird, Ron Petersen, David S. Knopman, Bradley F. Boeve, Dan Geschwind, Bruce L. Miller, Zbigniew K. Wszołek, Carol F. Lippa, Eileen H. Bigio, Dennis W. Dickson, Neill R. Graff‐Radford, Mike Hutton - The Lancet 2007 被引用: 218