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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...
Autores principales: | Murtinheira, Fernanda, Migueis, Mafalda, Letra-Vilela, Ricardo, Diallo, Mickael, Quezada, Andrea, Valente, Cláudia A., Oliva, Abel, Rodriguez, Carmen, Martin, Vanesa, Herrera, Federico |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
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 |
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