McGill researchers tackle rare disease first identified in Quebec | Faculty of Science - McGill University
PDF) Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy
MNI researchers receive funding to study ARSACS | The Neuro - McGill University
RCSB PDB - 5V46: Crystal structure of the I113M, F270M, K291M, L308M mutant of SR1 domain of human sacsin
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on
ARSACS OdV
News | ARSACS
ARSACS | Research That Heals
ARSACS OdV
Dall'Associazione ARSACS ODV un sostegno per i pazienti che aderiscono al progetto europeo PROSPAX - IRCCS Fondazione Stella Maris
Support the Foundation Arsacs | Italy Rome Tour
ARSACS | Research That Heals
Foundation/Fondation Arsacs | Montreal QC
Foundation/Fondation Arsacs | Montreal QC
Foundation/Fondation Arsacs | Montreal QC
ARSACS | Research That Heals
Sostenete la fondazione ARSACS ODV… Leggete perché! – SIAGASCOT
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
ARSACS | Research That Heals
Support the Foundation Arsacs | Italy Rome Tour
Research | ARSACS
ARSACS OdV
Research Project for Rare Disease Wins a Grant from ARSACS Foundation - imed
