SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Homozygous or compound heterozygous muta- tions in SACS gene a... | Download Table
Sacsin - Wikipedia
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
A Novel SACS Gene Mutation in a Tunisian Family | SpringerLink
Figure 2 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
Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS (sacsin molecular chaperone) | Gene Report | BioGPS
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
Human SACS Gene (Missense, Nonsense, and Frameshift Leading to... | Download Table
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) - ACNR | Paper & Online Neurology Journal ACNR | Paper & Online Neurology Journal
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
RNA-seq reveals conservation of function among the yolk sacs of human, mouse, and chicken | PNAS
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