Families and doctors team up to map rare genetic diseases
NCT ID NCT03303716
Summary
This study aims to better understand several rare genetic conditions caused by changes in ASXL genes. Researchers will collect health information over time from about 200 people who have one of these disorders. The goal is to learn about the typical course of these diseases and how they are currently managed to help guide future research and care.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of California, Los Angeles
RECRUITINGLos Angeles, California, 90095, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.