Direkt zum Inhalt wechseln

2nd European STXBP1 summit and research roundtable 2025

2nd European STXBP1 summit and research roundtable 2025

Wann

8. Oktober 2025 - 11. Oktober 2025    
0:00

The 2nd European STXBP1 Summit and Research Roundtable will be joined in 2025 in a unique event that will combine three crucial perspectives on STXBP1-Encephalopathy in Heidelberg, Germany. STXBP1-Encephalopathy has evolved to one of the most common causes for childhood neuro- developmental disorders, including the severe childhood epilepsies West syndrome, Lennox-Gastaut syndrome and other epileptic encephalopathies. The STXBP1 gene plays an important role in the neurosynaptic transmission. STXBP1 therapy research is a model disease of targeted therapies with new approaches from RNA/DNA gene replacement therapies.