Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)

Spinocerebellar ataxias (SCAs) constitute a heterogeneous group of more than 40 autosomal-dominant genetic and neurodegenerative diseases characterized by loss of balance and motor coordination due to dysfunction of the cerebellum and its efferent connections. Despite a well-described clinical and p...

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Detalles Bibliográficos
Autores principales: Prestori, Francesca, Moccia, Francesco, D’Angelo, Egidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981692/
https://www.ncbi.nlm.nih.gov/pubmed/31892274
http://dx.doi.org/10.3390/ijms21010216

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981692/
https://www.ncbi.nlm.nih.gov/pubmed/31892274
http://dx.doi.org/10.3390/ijms21010216

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