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The emerging role of autophagic-lysosomal dysfunction in Gaucher disease and Parkinson's disease
Gaucher disease (GD), the commonest lysosomal storage disorder, results from the lack or functional deficiency of glucocerebrosidase (GCase) secondary to mutations in the GBA1 gene. There is an established association between GBA1 mutations and Parkinson's disease (PD), and indeed GBA1 mutation...
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| Publicado no: | Neural Regen Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5399707/ https://ncbi.nlm.nih.gov/pubmed/28469644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1673-5374.202934 |
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