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Assessment of Sacsin Turnover in Patients With ARSACS: Implications for Molecular Diagnosis and Pathogenesis
BACKGROUND AND OBJECTIVES: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by variations in SACS gene encoding sacsin, a huge multimodular protein of unknown function. More than 200 SACS variations have been described worldwide to date. Because ARSACS presents phenotypic...
Autores principales: | Longo, Fabiana, De Ritis, Daniele, Miluzio, Annarita, Fraticelli, Davide, Baets, Jonathan, Scarlato, Marina, Santorelli, Filippo M., Biffo, Stefano, Maltecca, Francesca |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665432/ https://www.ncbi.nlm.nih.gov/pubmed/34649874 http://dx.doi.org/10.1212/WNL.0000000000012962 |
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