De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie Odile Krebs, Ridha Joober, Ronald G. Lafrenire, Jean Claude Lacaille, Laurent Mottron, Pierre Drapeau, Miriam H. Beauchamp, Michael S. Phillips, Eric Fombonne, Guy A. Rouleau, Jacques L. Michaud

Research output: Contribution to journal › Article › peer-review