Fig. 1From: Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardationSchematic representation of the FOXG1 protein and patient mutations. The DNA binding fork-head domain (FHD), the Groucho-binding domain (GBD), and the JARID1B binding domain (JBD) of FOXG1 are shown. The numbers below the protein refer to the amino acid positions, and the mutations are indicated by dotsBack to article page