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Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases
The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2003 by University of Heidelberg.
Recruitment status was  Recruiting
Study NCT00221832   Information provided by University of Heidelberg

First Received on September 14, 2005.   Last Updated on January 12, 2010   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Long QT Syndrome
Hypertrophic Cardiomyopathy
Additional conditions recognized in this trial
Arrhythmogenic Right Ventricular Dysplasia
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Hypertrophy
More general conditions related to this trial
Aortic Stenosis, Subvalvular
Aortic Valve Stenosis
Arrhythmias, Cardiac
Cardiovascular Abnormalities
Cardiovascular Diseases
Congenital Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Valve Diseases
Pathologic Processes
Pathological Conditions, Anatomical
Sponsors listed in this trial
University of Heidelberg


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