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Diseases

Genetic and Rare Diseases Information Center (GARD)

Spinocerebellar ataxia


Research

Clinical Trials & Research for this Disease

  • ClinicalTrials.gov lists trials that are studying or have studied Spinocerebellar ataxia. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.

Patient Registry

  • Coordination of Rare Diseases at Sanford (CoRDS) hosts a specific registry for patients with ataxia in partnership with the National Ataxia Foundation. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases. The CoRDS registry is free for patients to enroll and for researchers to access.
Other Names for this Disease
  • SCA
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