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

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