FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants

Mitter, D; Pringsheim, M; Kaulisch, M; Plumacher, KS; Schroder, S; Warthemann, R; Abou Jamra, R; Baethmann, M; Bast, T; Buttel, HM; Cohen, JS; Conover, E; Courage, C; Eger, A; Fatemi, A; Grebe, TA; Hauser, NS; Heinritz, W; Helbig, KL; Heruth, M; Huhl

Mitter, D (reprint author), Univ Hosp Leipzig, Inst Human Genet, Leipzig, Germany.

GENETICS IN MEDICINE, 2018; 20 (1): 98

Abstract

Purpose: The study aimed at widening the clinical and genetic spectrum and assessing genotype-phenotype associations in FOXG1 syndrome due to FOXG1 va......

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