| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8285447 | Parkinsonism & Related Disorders | 2018 | 5 Pages |
Abstract
We expand the phenotypic, genotypic, and ethnical spectrum of mutations in these genes. Our findings alert neurologists that rare genetic causes should be considered in complex phenotypes regardless of ethnicity.
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Authors
Humera Manzoor, Norbert Brüggemann, Hafiz Muhammad Jafar Hussain, Tobias Bäumer, Frauke Hinrichs, Muhammad Wajid, Alexander Münchau, Sadaf Naz, Katja Lohmann,