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 R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
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