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Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency

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Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency

Explore clinical trials studying Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency 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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