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Glucocerebrosidase Defects as a Major Risk Factor for Parkinson’s Disease
Heterozygous mutations of the GBA1 gene, encoding for lysosomal enzyme glucocerebrosidase (GCase), occur in a considerable percentage of all patients with sporadic Parkinson’s disease (PD), varying between 8% and 12% across the world. Genome wide association studies have confirmed the strong correla...
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| Udgivet i: | Front Aging Neurosci |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Frontiers Media S.A.
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7186450/ https://ncbi.nlm.nih.gov/pubmed/32372943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2020.00097 |
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