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Exploring the link between glucocerebrosidase mutations and parkinsonism
Clinical, genetic and pathological studies all demonstrate that mutations in glucocerebrosidase (GBA), which encodes the lysosomal enzyme deficient in Gaucher disease (GD), are an important and common risk factor for Parkinson disease (PD) and related disorders. Some patients with GD and Gaucher car...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3351003/ https://ncbi.nlm.nih.gov/pubmed/21723784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molmed.2011.05.003 |
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