Fig. 2From: Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)Position of MOGHE-related SLC35A2 variants along the protein. SLC35A2 protein schematic showing even distribution of somatic variants identified in MOGHE patients. Somatic recurrent variants are highlighted in bold blue. indel insertion and/or deletion, SNV single nucleotide variantBack to article page