Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants

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Veröffentlicht in:	Parkinsonism & related disorders 2023-02, Vol.107, p.105248-105248, Article 105248
Hauptverfasser:	Usnich, Tatiana, Olmedillas, Maria, Schell, Nathalie, Paul, Jefri J., Curado, Filipa, Skobalj, Snezana, Csoti, Ilona, Ertan, Sibel, Gruber, Doreen, Zittel, Simone, Sammler, Esther, Isaacson, Stuart H., Kühn, Andrea A., Pedrosa, David J., Reetz, Kathrin, Kasten, Meike, Rolfs, Arndt, Bauer, Peter, Skrahina, Volha, Klein, Christine, Brüggemann, Norbert
Format:	Artikel
Sprache:	eng
Schlagworte:	GBA risk variants Genetic Predisposition to Disease Genotype Glucosylceramidase - genetics Humans Mutation Non-motor symptoms Parkinson Disease - complications Parkinson Disease - genetics Parkinson's disease
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doi_str_mv	10.1016/j.parkreldis.2022.105248
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source	Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects	GBA risk variants Genetic Predisposition to Disease Genotype Glucosylceramidase - genetics Humans Mutation Non-motor symptoms Parkinson Disease - complications Parkinson Disease - genetics Parkinson's disease
title	Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants
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