Potential conflict of interest: None reported.
Effect of thalamotomy on focal hand dystonia in a family with DYT1 mutation†
Version of Record online: 29 SEP 2008
Copyright © 2008 Movement Disorder Society
Volume 23, Issue 15, pages 2251–2255, 15 November 2008
How to Cite
Kim, M. J., Jeon, S. R., Yoo, H.-W., Kim, G.-H., Lee, M. C. and Chung, S. J. (2008), Effect of thalamotomy on focal hand dystonia in a family with DYT1 mutation. Mov. Disord., 23: 2251–2255. doi: 10.1002/mds.22337
- Issue online: 24 NOV 2008
- Version of Record online: 29 SEP 2008
- Manuscript Accepted: 30 AUG 2008
- Manuscript Revised: 16 JUL 2008
- Manuscript Received: 15 APR 2008
- Korean Ministry of Health and Welfare. Grant Number: 01-PJ10-PG6-01GN15-0001
Additional Supporting Information may be found in the online version of this article.
|MDS_22337_sm_SuppFigure1.doc||149K||Supporting Information Figure 1. The results of mutation analysis of DYT1 gene. Family members, II:5, III:1, and III:4, revealed the presence of the GAG deletion. (A) The electrogram of heteroduplex assay. Abnormal shift bands in mutants are indicated by arrows. Bold letter indicated the affected. (B) Sequence analysis of the patient III:4. The GAG deletion site is indicated with bold underline and arrow. Normal control is shown in upper panel. Mutant allele, which mixed sequence with normal allele, is shown in lower panel for a patient.|
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