Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation

Spinocerebellar Ataxia type 6 (SCA6) is an autosomal dominant neurodegenerative disease characterized by late onset, slowly progressive, mostly pure cerebellar ataxia. It is one of three allelic disorders associated to CACNA1A gene, coding for the Alpha1 A subunit of P/Q type calcium channel Cav2.1...

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Detalles Bibliográficos
Autores principales: Giunti, Paola, Mantuano, Elide, Frontali, Marina, Veneziano, Liana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4329791/
https://www.ncbi.nlm.nih.gov/pubmed/25762895
http://dx.doi.org/10.3389/fncel.2015.00036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4329791/
https://www.ncbi.nlm.nih.gov/pubmed/25762895
http://dx.doi.org/10.3389/fncel.2015.00036

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