In collaboration with Dr. Michel Puceat (C2VN), this new project will explore the role of oligodendroglial cells in Cornelia de Lange syndrome, a rare multi-organ developmental disorder caused by mutations in the NIPBL gene, which encodes a cohesin DNA-loading protein. Given that most patients present neurological deficits, our goal is to better understand these impairments and develop strategies for prevention.

Special thanks to NeuroMarseille for their support.