A Prospective and Retrospective Registry and Biomarker Study to Evaluate the Natural History of Pediatric Patients with Cardiomyopathy due to MYBPC3 Mutations
Description
This is a natural history study.
Details
Age
Child
Eligibility
Children with a type of cardiomyopathy caused by a specific genetic mutation (MYBPC3 mutation) may be included in this research study.
Type of Study
Observational
Locations
Childrens Hospital Colorado
Principal Investigator
Stephanie Nakano, MD
Study ID
Protocol Number: 21-4206
Categories
Is this Study for You?
Not finding the right Study for you? Join ResearchMatch, a nation-wide registry connecting volunteers and researchers