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Glucocerebrosidase and Parkinson disease: Recent advances
Mutations of the glucocerebrosidase (GBA) gene are the most important risk factor yet discovered for Parkinson disease (PD). Homozygous GBA mutations result in Gaucher disease (GD), a lysosomal storage disorder. Heterozygous mutations have not until recently been thought to be associated with any pa...
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| Опубликовано в: : | Mol Cell Neurosci |
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| Главный автор: | |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2015
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4471139/ https://ncbi.nlm.nih.gov/pubmed/25802027 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2015.03.013 |
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