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Huntington’s Disease: Calcium Dyshomeostasis and Pathology Models
Huntington’s disease (HD) is a severe inherited neurodegenerative disorder characterized by motor dysfunction, cognitive decline, and mental impairment. At the molecular level, HD is caused by a mutation in the first exon of the gene encoding the huntingtin protein. The mutation results in an expand...
Autores principales: | Kolobkova, Y.A., Vigont, V.A., Shalygin, A.V., Kaznacheyeva, E.V. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508999/ https://www.ncbi.nlm.nih.gov/pubmed/28740725 |
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