FOXG1 Syndrome: Genotype–Phenotype Association in 84 Patients with FOXG1 Variants - Mitter, D.; Pringsheim, M.; Kaulisch, M.; Plümacher, K.; Schröder, S.; Warthemann, R.; Malzahn, D.; Zirn, B.; Brockmann, K. (Neuropediatrics, 2017)