Scientists launch registry to map rare genetic hearing loss
NCT ID NCT06680934
Summary
This study is creating a patient registry to gather detailed information from people with a specific genetic form of hearing loss caused by changes in the CABP2 gene. It aims to track the natural history of the condition by collecting genetic and clinical data, including hearing tests, from about 100 participants. The goal is to build a clearer picture of how this type of hearing loss develops over time to help guide future research.
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Study contacts
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Contact
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Locations
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University Medical Center Goettingen
RECRUITINGGöttingen, 37075, Germany
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
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