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ArticlesPeer ReviewedFull Text

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

Author / Creator:Rademakers, Rosa, PhD ; Baker, Matt, BSc ; Gass, Jennifer, BS ; Adamson, Jennifer, BS ; Huey, Edward D, MD ; Momeni, Parastoo, PhD ; Spina, Salvatore, MD ; Coppola, Giovanni, MD ; Karydas, Anna M, BA ; Stewart, Heather, PhD ; Johnson, Nancy, PhD ; Hsiung, Ging-Yuek, MD ; Kelley, Brendan, MD ; Kuntz, Karen, RN ; Steinbart, Ellen, MA ; Wood, Elisabeth McCarty, MS ; Yu, Chang-En, PhD ; Josephs, Keith, MD ; Sorenson, Eric, MD ; Womack, Kyle B, MD ; Weintraub, Sandra, PhD ; Pickering-Brown, Stuart M, PhD ; Schofield, Peter R, DSc ; Brooks, William S, MBBS ; Van Deerlin, Vivianna M, MD ; Snowden, Julie, PhD ; Clark, Christopher M, MD ; Kertesz, Andrew, MD ; Boylan, Kevin, MD ; Ghetti, Bernardino, MD ; Neary, David, FRCP ; Schellenberg, Gerard D, PhD ; Beach, Thomas G, FRCPC ; Mesulam, Marsel, MD ; Mann, David, PhD ; Grafman, Jordan, PhD ; Mackenzie, Ian R, MD ; Feldman, Howard, MD ; Bird, Thomas, MD ; Petersen, Ron, MD ; Knopman, David, MD ; Boeve, Bradley, MD ; Geschwind, Dan H, MD ; Miller, Bruce, MD ; Wszolek, Zbigniew, MD ; Lippa, Carol, MD ; Bigio, Eileen H, MD ; Dickson, Dennis, MD ; Graff-Radford, Neill, FRCP ; Hutton, Mike, PhD

Publisher:England: Elsevier Ltd

Journal title:Lancet neurology, 2007-10, Vol.6 (10), p.857-868

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

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

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