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IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11

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IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11

Explore clinical trials studying IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11 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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