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Spinocerebellar Ataxia, Autosomal Recessive 7

Clinical trial condition

Spinocerebellar Ataxia, Autosomal Recessive 7

Explore clinical trials studying Spinocerebellar Ataxia, Autosomal Recessive 7. Study availability and eligibility vary by location and protocol.

2 public trials 1 recruiting study

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Spinocerebellar Ataxia, Autosomal Recessive 7 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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Active, Not Recruiting

Longitudinal Assessment of Atypical Tripeptidyl Peptidase 1 Enzyme Deficiency Patients

NCT04098211

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +11 more
Locations: Children's Hospital of Orange County Orange, California, United States

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