| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10744976 | Parkinsonism & Related Disorders | 2015 | 4 Pages |
Abstract
In accordance with previous work, our data indicate that TUBB4A coding mutations do not play a critical role in the broad population of isolated dystonia patients. Rather, isolated dystonia as seen in DYT4 might be an exceptional feature occurring in the heterogeneous phenotypic spectrum due to TUBB4A mutations.
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Authors
Michael Zech, Sylvia Boesch, Angela Jochim, Sebastian Graf, Peter Lichtner, Annette Peters, Christian Gieger, Joerg Mueller, Werner Poewe, Bernhard Haslinger, Juliane Winkelmann,