Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene (Q58050234)
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Current Data About Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
(P31) (Q13442814)

(P50) (Q30500607)
(P1932) A. Zimprich
(P1545) 10

(Q21013476)
(P1932) C. Mannhalter
(P1545) 5

(P304) 1304-1305

(P407) (Q1860)

(P433) 8

(P478) 65

(P577) Monday, October 24, 2005

(P1433) (Q1161692)

(P1476) "Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene" (language: en)

(P2093) D. Haubenberger
(P1545) 1

R. E. Bittner
(P1545) 2

S. Rauch-Shorny
(P1545) 3

F. Zimprich
(P1545) 4

L. Wagner
(P1545) 6

I. Mineva
(P1545) 7

K. Vass
(P1545) 8

E. Auff
(P1545) 9

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External Links
(P356) 10.1212/01.WNL.0000180407.15369.92
(P698) 16247064