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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Dis Model Mech
Main Authors: 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.
Format: Artigo
Jezik:Inglês
Izdano: The Company of Biologists Ltd 2021
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8319550/
https://ncbi.nlm.nih.gov/pubmed/34160002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.048893
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki