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Childhood-onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia

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Childhood-onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia

Explore clinical trials studying Childhood-onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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Childhood-onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia trial results

Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

NCT01793168

Conditions: 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
Locations: Sanford Health Sioux Falls, South Dakota, United States

Online Patient Enrollment System Sydney, Australia

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