A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
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
Primary structure of the SACS gene (A) and domain organization of the... | 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
Sacsin - Wikipedia
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
Sacsin - Wikipedia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Novel compound heterozygous mutation in <fc>SACS</fc> gene leads to a milder autosomal recessive spastic ataxia of C
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
sacs gene - List of Frontiers' open access articles
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 R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon | Neurology
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
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i>SACS</i> mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala
