Progressive myoclonus epilepsy associated with SACS gene mutations | Neurology Genetics
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
RNA-seq reveals conservation of function among the yolk sacs of human, mouse, and chicken | PNAS
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
Table 1 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
SACS Home page
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
SACS Gene - GeneCards | SACS Protein | SACS Antibody
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
SACS (sacsin molecular chaperone) | Gene Report | BioGPS
SACS (sacsin molecular chaperone)
Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
Homozygous or compound heterozygous muta- tions in SACS gene a... | Download Table
Solved: 38. This Subcellular Structure Is An Extension Of ... | Chegg.com
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
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) - ACNR | Paper & Online Neurology Journal ACNR | Paper & Online Neurology Journal
A novel mutation in SACS gene in a family from southern Italy | Semantic Scholar
