Scientists hunt for heart defect genes in families
NCT ID NCT01192048
First seen Apr 13, 2026 · Last updated May 22, 2026 · Updated 7 times
Summary
This study aims to find the genetic causes of congenital heart disease, the most common birth defect. Researchers will use whole genome sequencing to analyze DNA from up to 5,000 people with the condition and their relatives. No treatment is offered; the goal is to better understand why these heart defects occur.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Nationwide Children's Hospital
RECRUITINGColumbus, Ohio, 43205, United States
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Conditions
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