Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative
50 auth. R. Rademakers, M. Baker, J. Gass, J. Adamson, E. Huey, P. Momeni, S. Spina, G. Coppola, A. Karydas, H. Stewart, N. Johnson, G. Hsiung, B. Kelley, Karen Kuntz, E. Steinbart, ... E. Wood, Chang-En Yu, K. Josephs, E. Sorenson, K. Womack, S. Weintraub, S. Pickering-Brown, P. Schofield, W. Brooks, V. Deerlin, J. Snowden, Christopher M. Clark, A. Kertesz, K. Boylan, B. Ghetti, D. Neary, G. Schellenberg, T. Beach, M. Mesulam, D. Mann, J. Grafman, I. Mackenzie, H. Feldman, T. Bird, Ron C. Petersen, D. Knopman, B. Boeve, D. Geschwind, B. Miller, Z. Wszolek, C. Lippa, E. Bigio, Dennis W. Dickson, N. Graff-Radford, M. Hutton