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Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)

Spinocerebellar ataxia type 31 (SCA31) is one of the autosomal-dominant neurodegenerative disorders that shows progressive cerebellar ataxia as a cardinal symptom. This disease is caused by a 2.5- to 3.8-kb-long complex pentanucleotide repeat containing (TGGAA)(n), (TAGAA)(n), (TAAAA)(n), and (TAAAA...

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Detalles Bibliográficos
Autores principales: Ishikawa, Kinya, Nagai, Yoshitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985187/
https://www.ncbi.nlm.nih.gov/pubmed/31755042
http://dx.doi.org/10.1007/s13311-019-00804-6