Inner retinal dysfunction in the autosomal recessive spastic ataxia of Charlevoix-Saguenay

• Main Authors: Borruat, F.-X, Holder, G.E, Bremner, F
• Other Authors: OPHTHALMOLOGY
• Format: Article
• Published: 2020
• Subjects: adult; Article; ataxic gait; autosomal recessive disorder; autosomal recessive spastic ataxia of Charlevoix Saguenay; case report; cerebellum atrophy; cerebellum vermis; clinical article; dysarthria; dysmetria; electroretinography; eye photography; gene; gene deletion; hereditary ataxia; homozygosity; human; keratoconus; male; nuclear magnetic resonance imaging; optical coherence tomography; retina bipolar ganglion cell; retina disease; SACS gene; spastic gait; spastic paraplegia; spinocerebellar degeneration; visual impairment; young adult
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/178138
• Institution: National University of Singapore

10.3389/fneur.2017.00523