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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

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

What is SACS Gene Spastic ataxia Charlevoix-Saguenay type NGS Genetic DNA  Test ?
What is SACS Gene Spastic ataxia Charlevoix-Saguenay type NGS Genetic DNA Test ?

Sacsin - Wikipedia
Sacsin - Wikipedia

SACS variants are a relevant cause of autosomal recessive hereditary motor  and sensory neuropathy | SpringerLink
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | SpringerLink

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

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

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

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

SACS Site Highlights
SACS Site Highlights

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

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

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 caused by novel  mutations in SACS gene: A report of two Chinese families - ScienceDirect
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect

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

Sacsin - Wikipedia
Sacsin - Wikipedia

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

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

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

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

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

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