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Myotonic dystrophy 1 (DM1) is an autosomal, dominantly inherited neuromuscular disorder characterized by skeletal muscle weakness, myotonia, cardiac conduction abnormalities, cataracts, and other abno...
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Lead Sponsor
Huashan Hospital
NCT06300307 · Myotonic Dystrophy 1
NCT05532813 · Steinert's Disease, Myotonic Dystrophy 1, and more
NCT07136844 · Neuromuscular Diseases, Obesity (Disorder), and more
NCT02398786 · Myotonic Dystrophy, Congenital Myotonic Dystrophy, and more
NCT07008469 · Myotonic Dystrophy Type 1, DM1, and more
Chinese People's Liberation Army General Hospital
Beijing, Beijing Municipality
Peking University First Hospital
Beijing, Beijing Municipality
First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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