ARSACS: Genetics and More - 23andMe
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
Sacsin - Wikipedia
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
SACS gene
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Site Highlights
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
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
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
