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Impaired Levels of Gangliosides in the Corpus Callosum of Huntington Disease Animal Models
Huntington Disease (HD) is a genetic neurodegenerative disorder characterized by broad types of cellular and molecular dysfunctions that may affect both neuronal and non-neuronal cell populations. Among all the molecular mechanisms underlying the complex pathogenesis of the disease, alteration of sp...
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| Publicado no: | Front Neurosci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5052274/ https://ncbi.nlm.nih.gov/pubmed/27766070 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2016.00457 |
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