Relevant conflicts of interest/financial disclosures: Nothing to report.
A Novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy
Article first published online: 22 FEB 2014
© 2014 International Parkinson and Movement Disorder Society
Volume 29, Issue 9, pages 1201–1204, August 2014
How to Cite
Araki, E., Tsuboi, Y., Daechsel, J., Milnerwood, A., Vilarino-Guell, C., Fujii, N., Mishima, T., Oka, T., Hara, H., Fukae, J. and Farrer, M. J. (2014), A Novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy. Mov. Disord., 29: 1201–1204. doi: 10.1002/mds.25833
Funding agencies: This research was undertaken, in part, thanks to funding from the Canada Excellence Research Chairs program (to M.J.F.). In addition, Leading Edge Endowment Funds provided by the Province of British Columbia, Life Labs, and Genome BC support the Dr. Donald Rix BC Leadership Chair (to M.J.F.).
Full financial disclosures and author roles may be found in the online version of this article.
- Issue published online: 18 AUG 2014
- Article first published online: 22 FEB 2014
- Manuscript Accepted: 9 DEC 2013
- Manuscript Revised: 29 OCT 2013
- Manuscript Received: 9 JUN 2013
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