FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum
Miriam S Reuter, Angelika Riess, Ute Moog, Tracy A Briggs, Kate E Chandler, Anita Rauch, Miriam Stampfer, Katharina Steindl, Dieter Gläser, Pascal Joset, DDD Study, Mandy Krumbiegel, Harald Rabe, Uta Schulte-Mattler, Peter Bauer, Stefanie Beck-Wödl, Jürgen Kohlhase, André Reis, Christiane Zweier
Journal of Medical Genetics Jan 2017, 54 (1) 64-72; DOI: 10.1136/jmedgenet-2016-104094