SLC13A5 Deficiency Natural History Study - United States Only
SLC13A5 Deficiency Natural History Study - United States Only
Enrolling by invitation · NCT06144957 · Registry updated 2025-08-05Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| SLC13A5 Deficiency Natural History Study - United States Only | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, amelocerebrohypohidrotic syndrome, brain disorder, central nervous system disorder, developmental and epileptic encephalopathy, 25, epilepsy, hereditary disease, movement disorder, nervous system disorder | Enrolling by invitation | Not stated | 2025-08-05 | NCT06144957 |
4 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Brown University | 104 |
| Stanford University | 620 |
| TESS Research Foundation | 3 |
| University of Texas Southwestern Medical Center | 295 |
3 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Brown University | Providence | United States | 8 |
| Lucille Packard Children's Hospital, Stanford University | Palo Alto | United States | 2 |
| University of Texas Southwestern Dallas | Dallas | United States | 1 |