A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia

Published 2009 View Full Article

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Title
A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia
Authors
Keywords
-
Journal
MUSCLE & NERVE
Volume 39, Issue 3, Pages 389-391
Publisher
Wiley
Online
2009-02-12
DOI
10.1002/mus.21225

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