SACS gene
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
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
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect
SACS Gene - GeneCards | SACS Protein | SACS Antibody
ARSACS DNA Test – DNA Access Lab
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
ARSACS: Genetics and More - 23andMe
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
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
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
