Genetic & Genomic MedicinemedRxivPreprint
Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2
Lottie D. Morison, Elisabeth Meffert, Miriam Stampfer…·Angela Tamsin Morgan
This study characterizes 29 individuals with FOXP2 variants, showing high prevalence of speech disorders and language impairments, with relatively specific phenotypes compared to other monogenic conditions.
DOI 10.1101/2022.06.01.22275851