Autosomal recessive spastic ataxia of Charlevoix-Saguenay
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
![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
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
SACS Home page
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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
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
SACS mutations. Graphical overview of mutations found in this and other... | 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
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
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
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
SACS Gene - GeneCards | SACS Protein | SACS Antibody
