Potential conflict of interest: Nothing to report.
Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion†
Version of Record online: 5 OCT 2010
Copyright © 2010 Movement Disorder Society
Volume 25, Issue 16, pages 2854–2857, 15 December 2010
How to Cite
De Carvalho Aguiar, P., Fuchs, T., Borges, V., Lamar, K.-M., Silva, S. M. A., Ferraz, H. B. and Ozelius, L. (2010), Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion. Mov. Disord., 25: 2854–2857. doi: 10.1002/mds.23133
- Issue online: 16 DEC 2010
- Version of Record online: 5 OCT 2010
- Manuscript Accepted: 9 MAR 2010
- Manuscript Revised: 27 NOV 2009
- Manuscript Received: 30 JUL 2009
- Dystonia Medical Research Foundation (LJO)
- Bachmann-Strauss Dystonia and Parkinson Foundation (LJO)
- National Institute of Neurological Disorders and Stroke. Grant Number: NS26636, LJO
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