IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
Mission®„¢ esiRNA for human SACS Gene - Tactical Tool for Gene Silencing | Procurenet Limited
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | Human Genetics
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacsin - Wikipedia
Frontiers | A Novel SACS Variant Identified in a Chinese Patient: Case Report and Review of the Literature
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 | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Sacsin - Wikipedia
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
