New alternative splicing variants of the ATXN2 transcript

BACKGROUND: Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder with progressive degeneration of cerebellar Purkinje cells and selective loss of neurons in the brainstem. This neurodegenerative disorder is caused by the expansion of a polyglutamine domain in ataxin-2. Ataxin-2 is...

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Detalles Bibliográficos
Autores principales: Lastres-Becker, Isabel, Nonis, David, Nowock, Joachim, Auburger, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650068/
https://www.ncbi.nlm.nih.gov/pubmed/33324888
http://dx.doi.org/10.1186/s42466-019-0025-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650068/
https://www.ncbi.nlm.nih.gov/pubmed/33324888
http://dx.doi.org/10.1186/s42466-019-0025-1

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