학술논문
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Document Type
Article
Author
Hanna, Michael G.; Houlden, Henry; Machado, Pedro M.; Gang, Qiang; Bettencourt, Conceicao; Healy, Estelle; Parton, Matthew; Holton, Janice L.; Brady, Stefen; Hilton-Jones, David; Shieh, Perry B.; Zanoteli, Edmar; de Camargo, Leonardo Valente; De Paepe, Boel; De Bleecker, Jan; Shaibani, Aziz; Ripolone, Michela; Violano, Raffaella; Moggio, Maurizio; Barohn, Richard J.; Dimachkie, Mazen M.; McVey, April L.; Pasnoor, Mamatha; Glenn, Melanie; Jawdat, Omar; Statland, Jeffrey; Rico, Gabrielle; Mora, Marina; Mantegazza, Renato; Zanotti, Simona; Needham, Merrilee; Mastaglia, Frank; Liang, Christina; Dalakas, Marinos C.; Biba, Angie; Chinoy, Hector; Lilleker, James B.; Lamb, Janine; Platt, Hazel; Cooper, Robert G.; Miller, James A.L.; Roberts, Mark; Househam, Elizabeth; Hilton, David; Shivane, Aditya; Bartlett, Amy; Kissel, John T.; Runk, Heidi; Wicklund, Matthew; Saperstein, David S.; McKinney, Lynette R.; Bettencourt, Conceição; Pittman, Alan M.; Hughes, Deborah; Singleton, Andrew B.
Source
In Neurobiology of Aging November 2016 47:218-218
Subject
Language
ISSN
0197-4580