Funding agencies: This study was supported by grants from The Ministry of Education and Science, Republic of Serbia (projects #ON175090 [to VK] and #ON175091 [to IN]), and a grant from the Hermann and Lilly Schilling Foundation (to CK).
De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient
Article first published online: 13 APR 2014
© 2014 International Parkinson and Movement Disorder Society
Volume 29, Issue 9, pages 1190–1193, August 2014
How to Cite
Dobričić, V., Kresojević, N., Westenberger, A., Svetel, M., Tomić, A., Ralić, V., Petrović, I., Lukić, M. J., Lohmann, K., Novaković, I., Klein, C. and Kostić, V. S. (2014), De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient. Mov. Disord., 29: 1190–1193. doi: 10.1002/mds.25876
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: 18 AUG 2014
- Article first published online: 13 APR 2014
- Manuscript Accepted: 27 JAN 2014
- Manuscript Revised: 13 JAN 2014
- Manuscript Received: 29 OCT 2013
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