| NCT ID | Title | Condition | Status | Updated |
|---|---|---|---|---|
| Not specified | ||||
| NCT01403402 | Congenital Muscle Disease Study of Patient and Family Reported Medical Information | Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency | Recruiting | 2021-08-09 |
Epilepsy (1)