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Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | PLOS ONE
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Gene - GeneCards | SACS Protein | SACS Antibody
ARSACS: Genetics and More - 23andMe
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
PDF] Autosomal recessive spastic ataxia of Charlevoix-Saguenay in a Portuguese child caused by a novel SACS mutation | Semantic Scholar
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
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 | ACNR Journal
SACS gene
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
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i>SACS</i> mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
ARSACS DNA Test – DNA Access Lab
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration