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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical Trial Readiness for the DystroglycanopathiesCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Malformations of Cortical Development, Group II, Muscular Disorders, Atrophic, autosomal recessive limb-girdle muscular dystrophy type 2I, autosomal recessive limb-girdle muscular dystrophy type 2M, central nervous system malformation, cerebral cortical dysplasia, cobblestone lissencephaly, eye disorder, hereditary disease, lissencephaly spectrum disorders, muscle tissue disorder, muscular dystrophy, muscular dystrophy-dystroglycanopathy, type A, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot stated2025-07-30NCT00313677

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Research sitesCityCountryLinked trials
University of Iowa, 200 Hawkins DriveIowa CityUnited States1