Scientists map rare brain disorder to pave way for First-Ever cures
Knowledge-focused
Recruiting now
This study aims to prepare for future clinical trials for STXBP1-related disorders, a rare and severe genetic condition causing seizures and developmental delays. Researchers will follow 120 patients over time to better understand how the disease progresses and to identify the be…
Sponsor: European STXBP1 Consortium • Aim: Knowledge-focused
Last updated Mar 30, 2026 14:30 UTC