Clinical and neuropathological features of progressive supranuclear palsy in Leucine rich repeat kinase (LRRK2) G2019S mutation carriers
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| Veröffentlicht in: | Movement disorders 2018-02, Vol.33 (2), p.335-338 |
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| container_end_page | 338 |
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| container_issue | 2 |
| container_start_page | 335 |
| container_title | Movement disorders |
| container_volume | 33 |
| creator | Vilas, Dolores Sharp, Madeleine Gelpi, Ellen Genís, David Marder, Karen S. Cortes, Etty Vonsattel, Jean‐Paul Tolosa, Eduard Alcalay, Roy N. |
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| doi_str_mv | 10.1002/mds.27225 |
| format | Article |
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| ispartof | Movement disorders, 2018-02, Vol.33 (2), p.335-338 |
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| language | eng |
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| source | MEDLINE; Wiley Journals |
| subjects | Aged Astrocytes - metabolism Astrocytes - pathology Glycine - genetics Humans Leucine Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics Locus Coeruleus - metabolism Locus Coeruleus - pathology LRRK2 protein Male Movement disorders Mutation - genetics Paralysis Progressive supranuclear palsy Serine - genetics Supranuclear Palsy, Progressive - genetics Supranuclear Palsy, Progressive - pathology tau Proteins - metabolism |
| title | Clinical and neuropathological features of progressive supranuclear palsy in Leucine rich repeat kinase (LRRK2) G2019S mutation carriers |
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