Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Autosomal recessive spastic ataxia of charlevoix-saguenay (ARSACS): Case report of a novel nonsense mutation in the SACS gene Agarwal A, Garg D, Kharat A, Qavi A - Ann Indian Acad Neurol
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
A novel mutation in SACS gene in a family from southern Italy | Semantic Scholar
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
Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
SACS Home page
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
Microarrays | Free Full-Text | SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia | HTML
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) - ACNR | Paper & Online Neurology Journal ACNR | Paper & Online Neurology Journal
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
SACS (sacsin molecular chaperone) | Gene Report | BioGPS
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish family – topic of research paper in Clinical medicine. Download scholarly
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody
