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

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 Site Highlights
SACS Site Highlights

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i>SACS</i> mutation-positive autosomal recessive spastic ataxia of  charlevoix saguenay (ARSACS) from Kerala
i>SACS</i> mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala

SACS mutations. Graphical overview of mutations found in this and other...  | Download Scientific Diagram
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram

SACS gene
SACS gene

Sacsin - Wikipedia
Sacsin - Wikipedia

Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... |  Download Scientific Diagram
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram

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

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

ARSACS: Genetics and More - 23andMe
ARSACS: Genetics and More - 23andMe

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

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

Pharmaceuticals | Free Full-Text | Discovery of Therapeutics Targeting  Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic  Review
Pharmaceuticals | Free Full-Text | Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review

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

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

IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of  Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration

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

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

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

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

A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... |  Download Scientific Diagram
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram