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Genetics of Cardiovascular and Neuromuscular Disease
Sponsor: University of Chicago
Summary
We are studying the genetics of human cardiovascular and neuromuscular disease. There are many different genetic regions that have been associated with the development of cardiomyopathy. An equal number of genetic regions have been associated with muscular dystrophy and there is overlap because some of the identical genes, when mutated, produce both cardiomyopathy and muscular dystrophy. We are working to identify genes and gene mutations associated with cardiomyopathy, arrhythmias and muscular dystrophy. We propose to screen these samples for mutations in genes known to be involved in these disorders.
Official title: Genetic Studies of Patients and Their Families With Inherited Cardiovascular and Neuromuscular Diseases.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
2000
Start Date
1996-09
Completion Date
2030-01
Last Updated
2025-09-09
Healthy Volunteers
No
Interventions
Blood draw (genetic testing)
Blood draw (genetic testing)
Locations (1)
University of Chicago
Chicago, Illinois, United States