Prospective investigation of FOXP1 syndrome

Siper, PM; De Rubeis, S; Trelles, MD; Durkin, A; Di Marino, D; Muratet, F; Frank, Y; Lozano, R; Eichler, EE; Kelly, M; Beighley, J; Gerdts, J; Wallace, AS; Mefford, HC; Bernier, RA; Kolevzon, A; Buxbaum, JD

Kolevzon, A (reprint author), Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, Friedman Brain Inst, Dept Psychiat,Dept Pediat, New York, NY 10029 USA.; Buxbaum, JD (reprint author), Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, Friedman Bra

MOLECULAR AUTISM, 2017; 8 ( ):

Abstract

Background: Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a neurodevelopmental disorder termed FOXP1 syndrome. Previous stud......

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