Complex Ataxia‐Dementia Phenotype in Patients with Digenic <i>TBP/STUB1</i> Spinocerebellar Ataxia

Abstract

The identification of the complex SCA^TBP/STUB1 phenotype may impact on diagnosis and genetic counseling in the families with both hereditary and sporadic ataxia. The independent segregation of TBP and STUB1 alleles needs to be considered for recurrence risk and predictive genetic tests. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.