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Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation

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Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation

Explore clinical trials studying Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation trial results

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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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