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
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
SACS Site Highlights
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Sacsin - Wikipedia
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
Frontiers | Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
ARSACS DNA Test – DNA Access Lab
SACS gene
Sacsin - Wikipedia
SACS Gene - GeneCards | SACS Protein | SACS Antibody
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
SACS Gene - GeneCards | SACS Protein | SACS Antibody
ARSACS: Genetics and More - 23andMe
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
A novel mutation in SACS gene in a family from southern Italy
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsinin Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
What is SACS Gene Spastic ataxia Charlevoix-Saguenay type NGS Genetic DNA Test ?
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | SpringerLink
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect
