Sacsin - Wikipedia
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | 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
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Primary structure of the SACS gene (A) and domain organization of the... | 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
Sacsin - Wikipedia
SACS Gene - GeneCards | SACS Protein | SACS Antibody
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
Genes | Free Full-Text | Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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 Gene - GeneCards | SACS Protein | SACS Antibody
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
ARSACS DNA Test – DNA Access Lab
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
A novel mutation in SACS gene in a family from southern Italy
SACS Site Highlights
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Potential effects of mutations in SACS gene. | Download Scientific Diagram
SACS gene
