Scientists hunt for genes behind rare kidney disease
NCT ID NCT01312727
First seen Jan 05, 2026 · Last updated May 01, 2026 · Updated 23 times
Summary
This study aims to find the genetic causes of a rare, inherited kidney disease called HTIN. Researchers will study 225 adults with the condition and their families to look for specific gene mutations. The goal is to better understand the disease, not to test a new treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Hôpital Necker Enfants Malades
Paris, 75015, France
Conditions
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