Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy
NCT01792960 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 99
Last updated 2014-02-19
Summary
Set the Korean Familial Hypertrophic Cardiomyopathy (KFHC) registry to study the prevalence of gene mutations in Korean patients with familial hypertrophic cardiomyopathy
Conditions
- Familial Hypertrophic Cardiomyopathy
Sponsors & Collaborators
-
Yonsei University
lead OTHER
Eligibility
- Min Age
- 13 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-02-28
- Primary Completion
- 2013-08-31
- Completion
- 2013-08-31
Countries
- South Korea
Study Locations
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