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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

A novel mutation in SACS gene in a family from southern Italy
A novel mutation in SACS gene in a family from southern Italy

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

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

Potential effects of mutations in SACS gene. | Download Scientific Diagram
Potential effects of mutations in SACS gene. | Download Scientific Diagram

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

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

Frontiers | Case Report: Expanding the Genetic and Phenotypic Spectrum of  Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Frontiers | Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

SACS gene
SACS gene

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

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

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

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

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

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

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

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

Insights into SACS pathological attributes in autosomal recessive spastic  ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect
Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect

Genes | Free Full-Text | Novel Variants in MPV17, PRX, GJB1, and SACS Cause  Charcot–Marie–Tooth and Spastic Ataxia of  Charlevoix–Saguenay Type Diseases
Genes | Free Full-Text | Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases

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

Sacsin - Wikipedia
Sacsin - Wikipedia

Sacsin - Wikipedia
Sacsin - Wikipedia

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

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

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