IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Research | ARSACS
News | ARSACS
Foundation/Fondation Arsacs | Montreal QC
ARSACS OdV
ARSACS OdV
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
Federico Herrera's project funded to study a rare neurodegenerative diagnosed in babies
National Ataxia Foundation (@NAF_Ataxia) / X
Interview with Sonia Gobeil, cofounder of the ARSACS Foundation | ARSACS
Foundation/Fondation Arsacs | Montreal QC
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
Research Project for Rare Disease Wins a Grant from ARSACAS Foundation
Foundation/Fondation Arsacs | Montreal QC
Reflecting on the 7th International ARSACS Symposium 2023 - Ataxia UK
Research Project for Rare Disease Wins a Grant from ARSACS Foundation - imed
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF | Nature Genetics
Foundation/Fondation Arsacs | Montreal QC
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
Support the Foundation Arsacs | Italy Rome Tour
Foundation/Fondation Arsacs | Montreal QC
ARSACS | Research That Heals
ARSACS | Research That Heals
ARSACS | Research That Heals
ARSACS | Research That Heals
