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Congenital Myotonic Dystrophy (CDM) is a multi-systemic, dominantly inherited disorder caused by a trinucleotide repeat expansion (CTGn) in the DMPK gene. CDM occurs when the CTGn increases between th...
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Lead Sponsor
Virginia Commonwealth University
Collaborators
NCT00082108 · Myotonic Dystrophy, Facioscapulohumeral Muscular Dystrophy, and more
NCT05004129 · Congenital Myotonic Dystrophy
NCT02398786 · Myotonic Dystrophy, Congenital Myotonic Dystrophy, and more
Virginia Commonwealth University
Richmond, Virginia
Pediatric Neuromuscular Research, Children's Hospital - LHSC
London, Ontario
Centro Clinico Nemo
Milan
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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