(Q46126082)
Statements
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A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia (English)
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Jochen Schaefer
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Dietrich Haubenberger
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Elisabeth Stogmann
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Eduard Auff
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1 March 2009
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39
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3
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389-391
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Identifiers
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