Massive gene hunt aims to unlock secrets of rare brain diseases
NCT ID NCT06072079
First seen Oct 31, 2025 · Last updated Apr 25, 2026 · Updated 18 times
Summary
This study looks at the DNA of 10,000 people with rare genetic disorders or brain conditions. Researchers will map out large DNA changes to find which genes cause disease. The goal is to improve genetic testing and pave the way for future treatments.
Disclaimer
Read more
Show less
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.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for RARE DISEASES are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Anna Lindstrand
Stockholm, 19175, Sweden
Conditions
Explore the condition pages connected to this study.