Letter to the Editor
Inclusion body myopathy with paget disease of bone and frontotemporal dementia associated with a novel G156s mutation in the VCP gene
Version of Record online: 30 OCT 2013
Copyright © 2013 Wiley Periodicals, Inc.
Muscle & Nerve
Volume 48, Issue 6, pages 995–996, December 2013
How to Cite
Komatsu, J., Iwasa, K., Yanase, D. and Yamada, M. (2013), Inclusion body myopathy with paget disease of bone and frontotemporal dementia associated with a novel G156s mutation in the VCP gene. Muscle Nerve, 48: 995–996. doi: 10.1002/mus.23960
- Issue online: 22 NOV 2013
- Version of Record online: 30 OCT 2013
- Accepted manuscript online: 19 JUL 2013 05:16AM EST
- Manuscript Accepted: 8 JUL 2013
- Manuscript Revised: 4 JUL 2013
- Manuscript Received: 19 JAN 2013
Additional Supporting Information may be found in the online version of this article.
|mus23960-sup-0001-suppfig1.tif||707K||Supporting Information Figure 1. Brain MRI showed bilateral frontotemporal lobe atrophy involving hippocampus and thickened bone of the skull.|
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