| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8285518 | Parkinsonism & Related Disorders | 2018 | 6 Pages |
Abstract
Point mutations in LRRK2 and SNCA are a rare cause of autosomal dominant PD in Turkey. However, copy number variations should be considered. The unclassified variants, especially LRRK2 R1067Q, demand further investigation.
Keywords
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Ageing
Authors
Christoph Kessler, Burcu Atasu, Hasmet Hanagasi, Javier Simón-Sánchez, Ann-Kathrin Hauser, Meltem Pak, Basar Bilgic, Nihan Erginel-Unaltuna, Hakan Gurvit, Thomas Gasser, Ebba Lohmann,