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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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Detalhes bibliográficos
Publicado no:Front Neurosci
Main Authors: Di Pardo, Alba, Amico, Enrico, Maglione, Vittorio
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2016
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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