Perry syndrome due to the DCTN1 G71R mutation: A distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure
Version of Record online: 1 APR 2010
Copyright © 2010 Movement Disorder Society
Volume 25, Issue 6, pages 767–770, 30 April 2010
How to Cite
Newsway, V., Fish, M., Rohrer, J. D., Majounie, E., Williams, N., Hack, M., Warren, J. D. and Morris, H. R. (2010), Perry syndrome due to the DCTN1 G71R mutation: A distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure. Mov. Disord., 25: 767–770. doi: 10.1002/mds.22950
- Issue online: 26 APR 2010
- Version of Record online: 1 APR 2010
- Manuscript Accepted: 12 NOV 2009
- Manuscript Revised: 11 NOV 2009
- Manuscript Received: 24 AUG 2009
- Medical Research Council (MRC)
- United Kingdom, Parkinson's disease society (United Kingdom)
- Wellcome Trust (United Kingdom)
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