Sacsin - Wikipedia
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
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Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE
ARSACS DNA Test – DNA Access Lab
Assessment of Sacsin Turnover in Patients With ARSACS | Neurology
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
SACS Site Highlights
SACS gene
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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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
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
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
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
Gene: SACS-AS1 (ENSG00000229558) - Summary - Homo_sapiens - GRCh37 Archive browser 108
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
