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AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency

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AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency

Explore clinical trials studying AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency. Study availability and eligibility vary by location and protocol.

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AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency trial results

Recruiting

A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders

NCT06092346

Conditions: ADA2 protein, human, ADA2, OMIM *607575,Sneddon Syndrome; VAIHS, ADSL, OMIM *608222, Adenylosuccinate Lyase Deficiency, +84 more
Locations: National Institutes of Health Clinical Center Bethesda, Maryland, United States

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