Massive 50,000-Person study unlocks secrets of rare genetic disorder
NCT ID NCT00500123
Summary
This study aims to understand the real-world use and impact of genetic testing for Alpha-1 Antitrypsin Deficiency, a rare inherited condition. It will enroll 50,000 people at risk for the disease to learn about who gets tested, why, and what happens afterward. The research focuses on gathering knowledge through confidential surveys and coded test results, not on providing treatment.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of Florida
RECRUITINGGainesville, Florida, 32610, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.