Interview with Sonia Gobeil, cofounder of the ARSACS Foundation | ARSACS
Federico Herrera's project funded to study a rare neurodegenerative diagnosed in babies
ARSACS | Research That Heals
National Ataxia Foundation (@NAF_Ataxia) / X
ARSACS OdV
Research Project for Rare Disease Wins a Grant from ARSACS Foundation - imed
ARSACS | Research That Heals
Foundation/Fondation Arsacs | Montreal QC
Support the Foundation Arsacs | Italy Rome Tour
McGill researchers tackle rare disease first identified in Quebec | Faculty of Science - McGill University
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
ARSACS | Research That Heals
ARSACS | Research That Heals
Foundation/Fondation Arsacs | Montreal QC
News | ARSACS
Sostenete la fondazione ARSACS ODV… Leggete perché! – SIAGASCOT
Foundation/Fondation Arsacs | Montreal QC
ARSACS OdV
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF | Nature Genetics
Dall'Associazione ARSACS ODV un sostegno per i pazienti che aderiscono al progetto europeo PROSPAX - IRCCS Fondazione Stella Maris
PDF) Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy
Research | ARSACS
Faces of ARSACS
Reflecting on the 7th International ARSACS Symposium 2023 - Ataxia UK
