A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
ARSACS: Genetics and More - 23andMe
ARSACS DNA Test – DNA Access Lab
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
Novel compound heterozygous mutation in <fc>SACS</fc> gene leads to a milder autosomal recessive spastic ataxia of C
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacsin - Wikipedia
SACS gene
![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
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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
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
Sacsin - Wikipedia
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
SACS Home page
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
