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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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| Опубликовано в: : | Front Aging Neurosci |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Frontiers Media S.A.
2020
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| Предметы: | |
| Online-ссылка: | 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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