Sacsin - Wikipedia
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
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Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
![PDF] Autosomal recessive spastic ataxia of Charlevoix-Saguenay in a Portuguese child caused by a novel SACS mutation | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/314bd6b198a74897ba2263295491662d666a5792/2-Figure1-1.png "PDF] Autosomal recessive spastic ataxia of Charlevoix-Saguenay in a Portuguese child caused by a novel SACS mutation | Semantic Scholar")
PDF] Autosomal recessive spastic ataxia of Charlevoix-Saguenay in a Portuguese child caused by a novel SACS mutation | Semantic Scholar
SACS gene
Sacsin - Wikipedia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon | Neurology
ARSACS DNA Test – DNA Access Lab
