Sacsin Deletion Induces Aggregation of Glial Intermediate Filaments

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder commonly diagnosed in infants and characterized by progressive cerebellar ataxia, spasticity, motor sensory neuropathy and axonal demyelination. ARSACS is caused by mutations in the SACS gene that lead...

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Detalles Bibliográficos
Autores principales: Murtinheira, Fernanda, Migueis, Mafalda, Letra-Vilela, Ricardo, Diallo, Mickael, Quezada, Andrea, Valente, Cláudia A., Oliva, Abel, Rodriguez, Carmen, Martin, Vanesa, Herrera, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773934/
https://www.ncbi.nlm.nih.gov/pubmed/35053415
http://dx.doi.org/10.3390/cells11020299

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773934/
https://www.ncbi.nlm.nih.gov/pubmed/35053415
http://dx.doi.org/10.3390/cells11020299

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