Scientists gather clues to unlock mysteries of rare genetic disorder
NCT ID NCT05202210
Summary
This study aims to create a collection of blood and urine samples from people with Noonan syndrome. The goal is to help researchers better understand how the disease works and find biological signs that might predict how severe it could become. The samples will be used for future research to improve knowledge about this rare genetic condition.
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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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Purpan University Hospital
RECRUITINGToulouse, 31059, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.