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Fragile X-associated Tremor/Ataxia Syndrome: A Feasibility Study of Measurement of Skin FMRpolyG

An Integrated Approach to Care Delivery for Patients with Hereditary Cerebellar Ataxia

Atypical Cerebrotendinous Xanthomatosis with Normal Serum Cholestanol and Novel VUS on the CYP27A1 Gene: A Case Report

Prevalence of FGF14-mediated Spinocerebellar Ataxia 27B (SCA27B) in a United States Cohort