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
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