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Neuronal Ca(2+) dyshomeostasis in Huntington disease
The expansion of the N-terminal poly-glutamine tract of the huntingtin (Htt) protein is responsible for Huntington disease (HD). A large number of studies have explored the neuronal phenotype of HD, but the molecular aethiology of the disease is still very poorly understood. This has hampered the de...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3609054/ https://ncbi.nlm.nih.gov/pubmed/23324594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.23581 |
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