| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8648088 | Blood Cells, Molecules, and Diseases | 2018 | 7 Pages |
Abstract
These middle-aged and older Swedish GD3 or GD1 patients are clinically stable over time. However, we have identified unusual clinical features, discordant phenotypes and a hyperkinetic dystonia-like movement disorder which appears unique to this Swedish disease variant and expands the phenotype for GD.
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Authors
Maciej Machaczka, Martin Paucar, Cecilia Kämpe Björkvall, Nicholas J.C. Smith, Timothy M Cox, Lars Forsgren, Per Svenningsson,