| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5504044 | Parkinsonism & Related Disorders | 2016 | 5 Pages |
Abstract
Our study does not allow the establishment of genotype-specific clinical correlations for DYT1. Further large-scale genetic screening accompanied by comprehensive segregation and functional studies is required to conclusively define the contribution of TOR1A whole-gene variation to the pathogenesis of isolated dystonia.
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Authors
Michael Zech, Angela Jochim, Sylvia Boesch, Sandrina Weber, Tobias Meindl, Annette Peters, Christian Gieger, Joerg Mueller, Michael Messner, Andres Ceballos-Baumann, Werner Poewe, Bernhard Haslinger, Juliane Winkelmann,