Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Q. Gang, C. Bettencourt, P.M. Machado, S. Brady, J.L. Holton, A.M. Pittman, D. Hughes, E. Healy, M. Parton, D. Hilton-Jones, P.B. Shieh, Merrilee Needham, C. Liang, E. Zanoteli, L.V. De Camargo, B. De Paepe, J. De Bleecker, A. Shaibani, M. Ripolone, R. ViolanoM. Moggio, R.J. Barohn, M.M. Dimachkie, M. Mora, R. Mantegazza, S. Zanotti, A.B. Singleton, M.G. Hanna, H. Houlden, A.L. Mcvey, M. Pasnoor, M. Glenn, O. Jawdat, J. Statland, G. Rico, F. Mastaglia, M.C. Dalakas, A. Biba, H. Chinoy, J.B. Lilleker, J. Lamb, H. Platt, R.G. Cooper, J.A.L. Miller, M. Roberts, E. Househam, D. Hilton, A. Shivane, A. Bartlett, J.T. Kissel, H. Runk, M. Wicklund, D.S. Saperstein, L.R. Mckinney

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27 Citations (Scopus)

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