Project
						Ongoing
						15 Members
			Phelan-McDermid Syndrome: from mechanisms to treatments
			Thomas Bourgeron (PI)
			Our team identified the first mutations in the SHANK3 gene, showing it’s role in autism and Phelan-McDermid Syndrome (PMS). Thanks to a donation from the French Association of Phelan-McDermid Syndrome, we will continue the […]