Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Titel:
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Auteur:
Gang, Qiang Bettencourt, Conceição Machado, Pedro M. Brady, Stefen Holton, Janice L. Pittman, Alan M. Hughes, Deborah Healy, Estelle Parton, Matthew Hilton-Jones, David Shieh, Perry B. Needham, Merrilee Liang, Christina 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. Mora, Marina Mantegazza, Renato Zanotti, Simona Singleton, Andrew B. Hanna, Michael G. Houlden, Henry
Verschenen in:
Neurobiology of aging
Paginering:
Jaargang 47 (2016) nr. C pagina's 2.17999997821E11 p.