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Clinical Trial Summary

After informed consent, participants will be asked to complete a medical/family history questionnaire and provide a blood sample. Participants will also be asked for their permission for study investigators to access medical records and/or recontact them for updates to their medical and family histories. Data and biospecimens will be stored for potential future research projects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00633607
Study type Observational
Source University of Pittsburgh
Contact
Status Completed
Phase N/A
Start date April 2012
Completion date January 26, 2018

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