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| GENATLAS PHENOTYPE |
| last update : 12-01-2013 |
| Symbol | DYT13 |
| Location | 1p36.32-p36.13 |
| HGNC id | 3101 |
| Name | dystonia 13, primary torsion |
| Main clinical features |
|
| Genetic determination | autosomal dominant |
| Function/system disorder | neurology |
| Type | disease |
| Remark(s) |