Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
University of Cologne · Philipps University of Marburg · +7 more institutions
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Abstract
No abstract available for this paper.
Citation impact
1,184
total citations
- FWCI
- 21.32
- Percentile
- 100%
- References
- 31
Citations per year
Authors
17Topics & keywords
Topics
Keywords
- Neurodegeneration
- Biology
- Parkinsonism
- Proteasome
- Endoplasmic reticulum
- Glucocerebrosidase
- Genetics
- Lysosome
UN Sustainable Development Goals
- Good health and well-being
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Funding
- TFTinker Foundation
- WTWellcome Trust
- RSRoyal Society
- DFDeutsche Forschungsgemeinschaft
- BFBundesministerium für Bildung und Forschung
- RFRheinische Friedrich-Wilhelms-Universität Bonn
- NINational Institutes of Health
- DFDirectorate for Biological Sciences
- NINational Institute of Child Health and Human Development