Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7

Spinocerebellar ataxia type 7 (SCA7) is an autosomal-dominant neurodegenerative disorder caused by a CAG repeat expansion in the coding region of the ataxin-7 gene. Infantile-onset SCA7 patients display extremely large repeat expansions (>200 CAGs) and exhibit progressive ataxia, dysarthria, dysp...

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Detalles Bibliográficos
Autores principales: Fusco, Anna F., Pucci, Logan A., Switonski, Pawel M., Biswas, Debolina D., McCall, Angela L., Kahn, Amanda F., Dhindsa, Justin S., Strickland, Laura M., La Spada, Albert R., ElMallah, Mai K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319550/
https://www.ncbi.nlm.nih.gov/pubmed/34160002
http://dx.doi.org/10.1242/dmm.048893

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319550/
https://www.ncbi.nlm.nih.gov/pubmed/34160002
http://dx.doi.org/10.1242/dmm.048893

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