Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Pharmaceuticals | Free Full-Text | Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review
Sacsin - Wikipedia
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsinin Neurodegeneration
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: Compound Heterozygotes for Nonsense Mutations of the SACS Gene - Vinodh Narayanan, Stephen G. Rice, Shannon S. Olfers, Kumaraswamy Sivakumar, 2011
i>SACS</i> mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala
Gene: SACS-AS1 (ENSG00000229558) - Summary - Homo_sapiens - GRCh37 Archive browser 108
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
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
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IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
SACS gene
ARSACS: Genetics and More - 23andMe
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
SACS Site Highlights
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
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
