| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8457457 | Neurologia i Neurochirurgia Polska | 2017 | 6 Pages |
Abstract
Reported cases confirm that the DRD phenotype may have heterogeneous genetic background and may be caused by point mutations or rearrangements in the GCH1 gene as well as in the PARK2 gene. Differential diagnosis and genetic tests covering the analysis of genes causative for DRD and EO-PD should be obligatory in both disorders diagnostics as DRD, mainly adolescent onset dystonia, may be associated with parkinsonism.
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Authors
Anna Potulska-Chromik, Dorota Hoffman-Zacharska, MaÅgorzata Åukawska, Anna Kostera-Pruszczyk,