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Clinical Trial Summary

Genetic mutations has been proved to be associated wth the onset of cardiomyopathy. In the present study, we intend to identify new related variants or genes. From March, 2003 to November, 2017, patients diagnosed as cardiomyopathy were consecutively recruited, and their sampled were drawn from peripheral blood. Paired control group were also enrolled. The whole exome sequencing was used to find out the variants associated with the onset of cardiomyopathy and its prognosis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03754101
Study type Observational
Source Tongji Hospital
Contact Chenze Li, MD candidate
Phone 86-27-83663280
Email lichenze@126.com
Status Recruiting
Phase
Start date March 3, 2003
Completion date October 31, 2025

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