Molecular and Genetic Studies of Congenital Myopathies
Molecular and Genetic Studies of Congenital Myopathies
Recruiting · NCT00272883 · Registry updated 2026-03-25Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Molecular and Genetic Studies of Congenital Myopathies | Congenital Fiber Type Disproportion, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Minicore Myopathy with External Ophthalmoplegia, Thomsen and Becker disease, central core myopathy, centronuclear myopathy, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not stated | 2026-03-25 | NCT00272883 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Boston Children's Hospital | 238 |
| Muscular Dystrophy Association | 11 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Genetics Division, Boston Children's Hospital | Boston | United States | 1 |