Glucocerebrosidase Mutations in Parkinson Disease
Following the discovery of a higher than expected incidence of Parkinson Disease (PD) in Gaucher disease, a lysosomal storage disorder, mutations in the glucocerebrocidase (GBA) gene, which encodes a lysosomal enzyme involved in sphingolipid degradation were explored in the context of idiopathic PD....
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SAGE Publishing
2017-08-01
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| Serie: | Journal of Parkinson’s Disease |
| Accesso online: | https://doi.org/10.3233/JPD-171092 |
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