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ATP Binding Cassette Subfamily D Member 3 Gene Mutation

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ATP Binding Cassette Subfamily D Member 3 Gene Mutation

Explore clinical trials studying ATP Binding Cassette Subfamily D Member 3 Gene Mutation. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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ATP Binding Cassette Subfamily D Member 3 Gene Mutation trial results

Recruiting

Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)

NCT01668186

Conditions: ACBD5 (AcylCoA Binding Domain 5) Deficiency, ATP Binding Cassette Subfamily D Member 3 Gene Mutation, Abnormalities, Multiple, +48 more
Locations: Research Institute of the McGill University Health Center Montreal, Quebec, Canada

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