Novel frameshift mutation in the SACS gene causing spastic ataxia of charlevoix-saguenay in a consanguineous family from the Arabian Peninsula: A case report and review of literature
Pharmaceuticals | Free Full-Text | Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family - Palmio - 2016 - Clinical Case Reports - Wiley Online Library
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
ARSACS: Genetics and More - 23andMe
Sacsin - Wikipedia
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Site Highlights
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology