Clinical and neuropathological features of progressive supranuclear palsy in Leucine rich repeat kinase (LRRK2) G2019S mutation carriers

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Bibliographische Detailangaben
Veröffentlicht in:	Movement disorders 2018-02, Vol.33 (2), p.335-338
Hauptverfasser:	Vilas, Dolores, Sharp, Madeleine, Gelpi, Ellen, Genís, David, Marder, Karen S., Cortes, Etty, Vonsattel, Jean‐Paul, Tolosa, Eduard, Alcalay, Roy N.
Format:	Artikel
Sprache:	eng
Schlagworte:	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
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