Mechanisms of USP7/MAGEL2 Complex Assembly and Its Mutational Disruption in Neurodevelopmental Diseases
Emilie J. Korchak, Gabriela Soriano, Irina Semenova, Bing Hao, Denis Štepihar, Tara Bayat, Klementina Fon Tacer, Irina Bezsonova
This study investigates the assembly mechanism of the USP7/MAGEL2 complex and identifies mutations that disrupt its formation, linking it to neurodevelopmental diseases.
bioRxiv · Apr 28, 2026 · PreprintBiochemistry