Scientists track rare blood disease across generations in search of answers
NCT ID NCT03854318
Summary
This study aims to learn more about a rare, inherited blood disorder called FPDMM, which is caused by a change in the RUNX1 gene. Researchers will follow 1,000 participants and their family members over many years to understand how the disease develops and changes over time. The goal is to gather information that could lead to better diagnosis, monitoring, and future treatments.
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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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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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