Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
SACS (sacsin molecular chaperone) | Gene Report | BioGPS
Solved: 38. This Subcellular Structure Is An Extension Of ... | Chegg.com
Human SACS Gene (Missense, Nonsense, and Frameshift Leading to... | Download Table
Sacsin - Wikipedia
SACS (sacsin molecular chaperone)
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
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala Sheetal S, Kumar S A, Byju P - Ann Indian Acad Neurol
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Microarrays | Free Full-Text | SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia | HTML
SACS Gene - GeneCards | SACS Protein | SACS Antibody
A Novel SACS Gene Mutation in a Tunisian Family | SpringerLink
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Home page
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
