Clinical Trials for Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)

Find clinical trials for alpha-dystroglycanopathy (congenital muscular dystrophy and abnormal glycosylation of dystroglycan with severe epilepsy). Discover research opportunities and treatment options in your area.

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Congenital Muscle Disease Study of Patient and Family Reported Medical Information

NCT ID: NCT01403402

The Congenital Muscle Disease Study, also known as CMDPROS, is a long-term research project aimed at understanding various types of congenital muscular dystrophy and related conditions. Over the ne...

Recruiting

Type: observational Locations: Lakewood, California, United States

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