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Nucleotide Repeat Disease clinical trials

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NCT ID: NCT04529252 Recruiting - Cerebellar Ataxia Clinical Trials

Investigating the Genetic and Phenotypic Presentation of Ataxia and Nucleotide Repeat Diseases

Start date: July 17, 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and phenotypic presentations of both.