RNA-seq reveals conservation of function among the yolk sacs of human, mouse, and chicken | PNAS
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
Homozygous or compound heterozygous muta- tions in SACS gene a... | Download Table
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
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
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
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) - ACNR | Paper & Online Neurology Journal ACNR | Paper & Online Neurology Journal
SACS (sacsin molecular chaperone)
Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
SACS Gene - GeneCards | SACS Protein | SACS Antibody
A novel mutation in SACS gene in a family from southern Italy | Semantic Scholar
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Sacsin - Wikipedia
SACS Home page
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
Human SACS Gene (Missense, Nonsense, and Frameshift Leading to... | Download Table
SACS mutation-positive autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS) from Kerala Sheetal S, Kumar S A, Byju P - Ann Indian Acad Neurol
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Human SACS Gene (Missense, Nonsense, and Frameshift Leading to... | Download Table
SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody
