Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
ARSACS DNA Test – DNA Access Lab
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Potential effects of mutations in SACS gene. | Download Scientific Diagram
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect
ARSACS: Genetics and More - 23andMe
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
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Identification of a SACS gene missense mutation in ARSACS | Neurology
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
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
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Sacsin - Wikipedia
SACS Gene - GeneCards | SACS Protein | SACS Antibody
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | Human Genetics
Frontiers | Genomic identification of cotton SAC genes branded ovule and stress-related key genes in Gossypium hirsutum
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
Frontiers | A Novel SACS Variant Identified in a Chinese Patient: Case Report and Review of the Literature
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
