Mission®„¢ esiRNA for human SACS Gene - Tactical Tool for Gene Silencing | Procurenet Limited
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
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
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
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
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
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
ARSACS DNA Test – DNA Access Lab
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS gene
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Potential effects of mutations in SACS gene. | Download Scientific Diagram
Frontiers | A Novel SACS Variant Identified in a Chinese Patient: Case Report and Review of the Literature
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | Human Genetics
SACS Gene - GeneCards | SACS Protein | SACS Antibody
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
ARSACS: Genetics and More - 23andMe
Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
