Integrative Organelle-Based Functional Proteomics: In Silico Prediction of Impaired Functional Annotations in SACS KO Cell Model

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an inherited neurodegenerative disease characterized by early-onset spasticity in the lower limbs, axonal-demyelinating sensorimotor peripheral neuropathy, and cerebellar ataxia. Our understanding of ARSACS (genetic basis, protein...

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Detalles Bibliográficos
Autores principales: Morani, Federica, Doccini, Stefano, Galatolo, Daniele, Pezzini, Francesco, Soliymani, Rabah, Simonati, Alessandro, Lalowski, Maciej M., Gemignani, Federica, Santorelli, Filippo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331974/
https://www.ncbi.nlm.nih.gov/pubmed/35892334
http://dx.doi.org/10.3390/biom12081024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331974/
https://www.ncbi.nlm.nih.gov/pubmed/35892334
http://dx.doi.org/10.3390/biom12081024

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