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Beyond Krabbe’s disease: the potential contribution of GALC deficiency to neuronal vulnerability in late onset synucleinopathies
New insights into the pathophysiological mechanisms behind late onset neurodegenerative diseases have come from unexpected sources in recent years. Specifically, the group of inherited metabolic disorders known as lysosomal storage diseases that most commonly affect infants has been found to have su...
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| Publicat a: | J Neurosci Res |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5027968/ https://ncbi.nlm.nih.gov/pubmed/27638614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.23751 |
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