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A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders
- National Institutes of Health Clinical Center, Bethesda
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1 Month – 100 Years · Saalaa hunda · Haaromfame 19-Hag-2026 · NCT06092346Inherited Retinal Degenerative Disease Registry
- Foundation Fighting Blindness, Columbia
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Umuriin hundi · Saalaa hunda · Haaromfame 19-Cam-2026 · NCT02435940The Myelin Disorders Biorepository Project
- Kennedy Krieger Institute, Baltimore
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Umuriin hundi · Saalaa hunda · Haaromfame 23-Onk-2025 · NCT03047369Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
- Johns Hopkins University, Baltimore
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Umuriin hundi · Saalaa hunda · Haaromfame 07-Onk-2025 · NCT01193088Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others
- Johns Hopkins University, Baltimore
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Umuriin hundi · Saalaa hunda · Haaromfame 07-Onk-2025 · NCT01193075Kanneen ClinicalTrials.gov irraa argaman, daataa 06-Onk-2026 irratti argame. Qorannoon hundi isaa kan ofii qajeelfama qoodfannaa qaba; gareen qorannoo eenyu akka hirmaatu murteessa.