Research & Innovation
Publications
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
PMU Author
Gerhard Kluger
All Authors
Diana Mitter, Milka Pringsheim, Marc Kaulisch, Kim Sarah Plümacher, Simone Schröder, Rita Warthemann, Rami Abou Jamra, Martina Baethmann, Thomas Bast, Hans-Martin Büttel, Julie S Cohen, Elizabeth Conover, Carolina Courage, Angelika Eger, Ali Fatemi, Theresa A Grebe, Natalie S Hauser, Wolfram Heinritz, Katherine L Helbig, Marion Heruth, Dagmar Huhle, Karen Höft, Stephanie Karch, Gerhard Kluger, G Christoph Korenke, Johannes R Lemke, Richard E Lutz, Steffi Patzer, Isabelle Prehl, Konstanze Hoertnagel, Keri Ramsey, Tina Rating, Angelika Rieß, Luis Rohena, Mareike Schimmel, Rachel Westman, Frank-Martin Zech, Barbara Zoll, Dörthe Malzahn, Birgit Zirn, Knut Brockmann
Journal association
GENETICS IN MEDICINE
Abstract
Keywords
GENE, FEATURES, MUTATIONS, EPILEPSY, DISORDER, RETT-SYNDROME, HAPLOINSUFFICIENCY, CONGENITAL VARIANT, SEVERE MENTAL-RETARDATION, 14Q12