Funding agencies: This work was supported in part by the Genetic Network for Hereditary Movement Disorders (GeNeMove, 01GM0304, http://www.genemove.org), funded by the German Ministry for Education and Research (GMER, BMBF), and by research grants from the German Research Foundation (LO1555/3-1 to Katja Lohmann), the Hermann and Lilly Schilling Foundation, and the Volkswagen Foundation (to Christine Klein).
Letters: New Observation
Article first published online: 2 JUN 2011
Copyright © 2011 Movement Disorder Society
Volume 26, Issue 11, pages 2136–2137, September 2011
How to Cite
Kamm, C., Uflacker, N., Asmus, F., Schrader, C., Wolters, A., Wittstock, M., Pahnke, J., Gasser, T., Volkmann, J., Münchau, A., Hagenah, J., Benecke, R., Klein, C. and Lohmann, K. (2011), No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia. Mov. Disord., 26: 2136–2137. doi: 10.1002/mds.23777
Relevant conflicts of interest/financial disclosures: Nothing to report.
Full financial disclosures and author roles may be found in the online version of this article.
- Issue published online: 19 SEP 2011
- Article first published online: 2 JUN 2011
- Manuscript Accepted: 8 APR 2011
- Manuscript Revised: 2 APR 2011
- Manuscript Received: 21 JAN 2011