Genetics Division, Boston Children's Hospital

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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

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