Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
![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
ARSACS DNA Test – DNA Access Lab
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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 - List of Frontiers' open access articles
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
SACS gene
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
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
SACS Home page
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
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
ARSACS: Genetics and More - 23andMe
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon | Neurology
Novel compound heterozygous mutation in <fc>SACS</fc> gene leads to a milder autosomal recessive spastic ataxia of C
Sacsin - Wikipedia
