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Sacsin cotranslational degradation causes autosomal recessive spastic  ataxia of Charlevoix-Saguenay | bioRxiv
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody

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
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

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
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

IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related  Disease Phenotypes in Zebrafish
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish

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Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology

Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian  Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay |  PLOS ONE
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE

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 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 Site Highlights
SACS Site Highlights

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody

R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... |  Download Scientific Diagram
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram

Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay  (ARSACS) and Role of Sacsinin Neurodegeneration
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
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics

SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients

ARSACS DNA Test – DNA Access Lab
ARSACS DNA Test – DNA Access Lab

Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay  (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic  Scholar
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal

Primary structure of the SACS gene (A) and domain organization of the... |  Download Scientific Diagram
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram

Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular  Brain | Full Text
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text

Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology

SACS gene
SACS gene

Gene: SACS-AS1 (ENSG00000229558) - Summary - Homo_sapiens - GRCh37 Archive  browser 108
Gene: SACS-AS1 (ENSG00000229558) - Summary - Homo_sapiens - GRCh37 Archive browser 108

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody