In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 .
Lottie D MorisonElisabeth MeffertMiriam StampferIrene Steiner-WilkeBrigitte VollmerKatrin SchulzeTracy BriggsRuth BradenAdam P VogelDaisy Thompson-LakeChirag PatelEdward BlairHimanshu GoelSamantha TurnerUte MoogAngelika RiessFrederique LiegeoisDavid A KoolenDavid J AmorTjitske KleefstraSimon E FisherChristiane ZweierAngela T MorganPublished in: Journal of medical genetics (2022)
provides a valuable entry point for examining the neurobiological bases of speech disorder.