Funding agencies: This work was supported by Grants-in-Aid from the Dystonia Research Committee, Ministry of Health, Labor, and Welfare of Japan (to R.K.); the Funding Program for Next-Generation, World-Leading Researchers from the Cabinet Office, Government of Japan; a Grant-in-Aid for Scientific Research on Innovative Areas (Brain Environment) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to H.Maruyama); and a Grant-in-Aid from the Research Committee of Central Nervous System Degenerative Diseases, the Ministry of Health, Labor, and Welfare of Japan (to H.Kawakami).
Letters: New Observations
DYT6 in Japan—genetic screening and clinical characteristics of the patients
Version of Record online: 13 NOV 2013
© 2013 Movement Disorder Society
Volume 29, Issue 2, pages 278–280, February 2014
How to Cite
Miyamoto, R., Koizumi, H., Morino, H., Kawarai, T., Maruyama, H., Mukai, Y., Miyashiro, A., Sako, W., Izumi, Y., Kawakami, H. and Kaji, R. (2014), DYT6 in Japan—genetic screening and clinical characteristics of the patients. Mov. Disord., 29: 278–280. doi: 10.1002/mds.25745
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 online: 20 FEB 2014
- Version of Record online: 13 NOV 2013
- Manuscript Accepted: 21 OCT 2013
- Manuscript Revised: 6 OCT 2013
- Manuscript Received: 18 AUG 2013
Additional Supporting Information may be found in the online version of this article.
|mds25745-sup-0001-suppinfo01.mp4||12031K||Supplementary Information Video 1|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.