Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice

Pringsheim, M; Mitter, D; Schroder, S; Warthemann, R; Plumacher, K; Kluger, G; Baethmann, M; Bast, T; Braun, S; Buttel, HM; Conover, E; Courage, C; Datta, AN; Eger, A; Grebe, TA; Hasse-Wittmer, A; Heruth, M; Hoft, K; Kaindl, AM; Karch, S; Kautzky, T;

Brockmann, K (reprint author), Univ Med Ctr Gottingen, Interdisciplinary Pediat Ctr Children Dev Disabil, Robert Koch Str 40, D-37075 Gottingen, Germany.

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2019; 6 (4): 655

Abstract

Objective FOXG1 syndrome is a rare neurodevelopmental disorder associated with heterozygous FOXG1 variants or chromosomal microaberrations in 14q12. T......

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