Disease progression of spinocerebellar ataxia types 1, 2, 3 and 6 before and after ataxia onset.
Heike JacobiTamara SchaprianTanja Schmitz-HübschMatthias SchmidThomas Klockgethernull nullPublished in: Annals of clinical and translational neurology (2023)
Our data have important implications for the understanding of disease progression in SCA1, SCA2, SCA3 and SCA6 across the lifespan. Furthermore, our study provides information for the design of interventional trials, especially in pre-ataxic mutation carriers close to ataxia onset and patients in early disease stages.