| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5502525 | Journal of the Neurological Sciences | 2017 | 7 Pages |
Abstract
Our results show that a common polymorphism in the PITX3 gene affects the risk of developing PDD and visuospatial dysfunction in idiopathic PD. If validated, these findings can provide new insights into the neurobiology and genetics of non-motor symptoms in PD.
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Authors
David Bäckström, Magdalena Eriksson Domellöf, Gabriel GranÃ¥sen, Jan Linder, Sofia Mayans, Eva Elgh, Susanna Jakobson Mo, Lars Forsgren,