De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
FOXP1基因的新生突变与智力障碍、自闭症和语言障碍有关
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2010.09.017
Hamdan, Fadi F; Daoud, Hussein; Rochefort, Daniel; Piton, Amélie; Gauthier, Julie; Langlois, Mathieu; Foomani, Gila; Dobrzeniecka, Sylvia; Krebs, Marie-Odile; Joober, Ridha; Lafrenière, Ronald G; Lacaille, Jean-Claude; Mottron, Laurent; Drapeau, Pierre; Beauchamp, Miriam H; Phillips, Michael S; Fombonne, Eric; Rouleau, Guy A; Michaud, Jacques L