https://www.selleckchem.com/pr....oducts/DAPT-GSI-IX.h
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) causes unique retinal abnormalities, which have not been systematically investigated. To deeply phenotype the retina in ARSACS in order to better understand its pathogenesis and identify potential biomarkers. We evaluated 29 patients with ARSACS, 66 with spinocerebellar ataxia (SCA), 38 with autosomal recessive cerebellar ataxia (ATX), 22 with hereditary spastic paraplegia (SPG), 21 cases of papilledema, and 20 healthy controls (total n = 196 subjects). Participants
Like
Comment
Share
