SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Microarrays | Free Full-Text | SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia | HTML
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
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
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS (sacsin molecular chaperone)
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
Sacsin - Wikipedia
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
Solved: 38. This Subcellular Structure Is An Extension Of ... | Chegg.com
Human SACS Gene (Missense, Nonsense, and Frameshift Leading to... | Download Table
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
SACS Home page
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 R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
Sacsin - Wikipedia
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
Homozygous or compound heterozygous muta- tions in SACS gene a... | Download Table
SACS Gene - GeneCards | SACS Protein | SACS Antibody
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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
