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

✍ Scribed by 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 Hsiung; Brendan Kelley; Karen Kuntz; Ellen Steinbart; Elisabeth McCarty Wood; Chang-En Yu; Keith Josephs; Eric Sorenson; Kyle B Womack; Sandra Weintraub; Stuart M Pickering-Brown; Peter R Schofield; William S Brooks; Vivianna M Van Deerlin; Julie Snowden; Christopher M Clark; Andrew Kertesz; Kevin Boylan; Bernardino Ghetti; David Neary; Gerard D Schellenberg; Thomas G Beach; Marsel Mesulam; David Mann; Jordan Grafman; Ian R Mackenzie; Howard Feldman; Thomas Bird; Ron Petersen; David Knopman; Bradley Boeve; Dan H Geschwind; Bruce Miller; Zbigniew Wszolek; Carol Lippa; Eileen H Bigio; Dennis Dickson; Neill Graff-Radford; Mike Hutton

• Book ID: 114408719
• Publisher: The Lancet
• Year: 2007
• Tongue: English
• Weight: 173 KB
• Volume: 6
• Category: Article
• ISSN: 1474-4465
• DOI: 10.1016/s1474-4422(07)70221-1