Relevant conflicts of interest/financial disclosures: Nothing to report.
Letters: New Observation
Phenotypic variability in a dystonia family with mutations in the manganese transporter gene
Version of Record online: 16 APR 2013
Copyright © 2013 Movement Disorder Society
Volume 28, Issue 5, pages 685–686, May 2013
How to Cite
Delnooz, C. C. S., Wevers, R. A., Quadri, M., Clayton, P. T., Mills, P. B., Tuschl, K., Steenbergen, E. J., Bonifati, V. and van de Warrenburg, B. P. C. (2013), Phenotypic variability in a dystonia family with mutations in the manganese transporter gene. Mov. Disord., 28: 685–686. doi: 10.1002/mds.25390
Full financial disclosures and author roles may be found in the online version of this article.
- Issue online: 15 MAY 2013
- Version of Record online: 16 APR 2013
- Manuscript Accepted: 15 JAN 2013
- Manuscript Revised: 3 JAN 2013
- Manuscript Received: 17 JUN 2012
No abstract is available for this article.