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GBA1 mutations: Prospects for Exosomal Biomarkers in α-Synuclein Pathologies
The discovery that patients with Gaucher Disease (GD), a rare lysosomal storage disorder, were developing symptoms similar to Parkinson Disease (PD) led to investigation of the relationship between the two seemingly unrelated pathologies. GD, an autosomal recessive disorder, is the result of a biall...
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| Publicado no: | Mol Genet Metab |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7002237/ https://ncbi.nlm.nih.gov/pubmed/31761523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2019.10.006 |
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